Hamari Chemicals, Ltd.

Japan

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IPC Class
C07B 53/00 - Asymmetric syntheses 9
C07B 61/00 - Other general methods 4
A61P 43/00 - Drugs for specific purposes, not provided for in groups 3
C07C 227/32 - Preparation of optical isomers by stereospecific synthesis 3
C07C 229/36 - Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings with at least one amino group and one carboxyl group bound to the same carbon atom of the carbon skeleton 3
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NICE Class
01 - Chemical and biological materials for industrial, scientific and agricultural use 11
05 - Pharmaceutical, veterinary and sanitary products 11
40 - Treatment of materials; recycling, air and water treatment, 3
42 - Scientific, technological and industrial services, research and design 3
03 - Cosmetics and toiletries; cleaning, bleaching, polishing and abrasive preparations 2
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Status
Pending 3
Registered / In Force 29

1.

CONTINUOUS LIQUID SEPARATING APPARATUS AND CONTINUOUS LIQUID SEPARATING METHOD

      
Application Number 18137674
Status Pending
Filing Date 2023-04-21
First Publication Date 2023-10-26
Owner Hamari Chemicals, Ltd. (Japan)
Inventor
  • Masuda, Shigeaki
  • Ohira, Masayuki
  • Kawamoto, Tetsuji
  • Ishihara, Yuji

Abstract

The continuous liquid separation is a continuous liquid separating apparatus that separates a first liquid and a second liquid that is immiscible to the first liquid and has a higher specific gravity than the first liquid, and includes: a liquid separating tank configured to contain a liquid, and be supplied with a liquid mixture of the first liquid and the second liquid, and including a first discharge portion on a lower side thereof and a second discharge portion disposed at a position higher than the first discharge portion, a valve configured to open/close the first discharge portion, a first sensor configured to detect a first water level of the liquid mixture contained in the liquid separating tank, the first water level being lower than the second discharge portion, and a second sensor configured to detect a second water level of the liquid mixture contained in the liquid separating tank.

IPC Classes  ?

  • B01D 17/02 - Separation of non-miscible liquids
  • B01D 17/12 - Auxiliary equipment particularly adapted for use with liquid-separating apparatus, e.g. control circuits
  • G01F 23/292 - Light

2.

Miscellaneous Design

      
Application Number 1692803
Status Registered
Filing Date 2022-03-03
Registration Date 2022-03-03
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ?
  • 01 - Chemical and biological materials for industrial, scientific and agricultural use
  • 03 - Cosmetics and toiletries; cleaning, bleaching, polishing and abrasive preparations
  • 05 - Pharmaceutical, veterinary and sanitary products
  • 30 - Basic staples, tea, coffee, baked goods and confectionery
  • 40 - Treatment of materials; recycling, air and water treatment,
  • 42 - Scientific, technological and industrial services, research and design

Goods & Services

Chemicals; industrial chemicals; chemicals used in science; plant extracts for use in the manufacture of pharmaceuticals; plant extracts for use in the manufacture of cosmetics; plant extracts for use in the manufacture of food; chemical additives for use in the manufacture of food; animal extracts for use in manufacture of pharmaceuticals; animal extracts for use in manufacture of cosmetics; animal extracts for use in the manufacture of foods; glues and adhesives for industrial purposes; plant growth regulating preparations; chemicals used in agriculture, horticulture and forestry; fertilizers; ceramic glazings; oil cement [putty]; higher fatty acids; fatty acids for industrial purpose; non-metallic minerals; non-metallic minerals for use in manufacture; photographic chemicals; photographic developers; reagent paper [not for medical purposes]; reagent paper, other than for medical or veterinary purposes; artificial sweeteners; artificial sweeteners [chemical preparations]; flour and starch for industrial purposes; plastics [raw materials]; plastics, unprocessed; paper pulp, cellulose pulp, wood pulp; paper pulp; dissolving pulp. Anti-static preparations for household purposes; de-greasing preparations for household purposes; rust removing preparations; stain removing benzine; fabric softeners for laundry use; laundry bleach; adhesives for affixing false hair; laundry starch; seaweed gelatine for laundry use [Funori]; adhesives for affixing false eyelashes; breath freshening preparations; breath freshening preparations for personal hygiene; deodorants for animals; paint stripping preparations; shoe cream; shoe black [shoe polish]; polishing preparations; soaps and detergents; bar soap; bath soaps; liquid soap; detergent soap; detergents for household use; dentifrices; cosmetics; perfumes and fragrances; perfumes; perfumes for industrial purposes; essential oils for use as food and drink flavorings; essential oils; body deodorant cosmetics and fragrances; fragrances; incense; abrasive paper; abrasive cloth; abrasive sand; artificial pumice stone; polishing paper; false nails; false eyelashes. Pharmaceutical preparations and other preparations for destroying vermin, fungicides, herbicides; pharmaceutical preparations; pharmaceutical, medical and veterinary preparations; chemical reagents for medical or veterinary purposes; vitamin preparations; nutritional additives; disinfectants; preparations for destroying vermin; fungicides; herbicides; plant extracts for pharmaceutical purposes; nutritional supplement drinks; nursing tonic nutritional supplement drinks; nutritional supplement beverage; reagent paper for medical purposes; oiled paper for medical purposes; adhesive tapes for medical purposes; drug delivery agents in the form of edible wafers for wrapping powdered pharmaceuticals; gauze for dressings; empty capsules for pharmaceuticals; eyepatches for medical purposes; ear bandages; menstruation bandages; menstruation tampons; sanitary napkins; sanitary panties; absorbent cotton; adhesive plasters; bandages for dressings; liquid bandages; liquid bandages for skin wounds; breast-nursing pads; cotton swabs for medical use; dental materials; diapers; diaper covers; mothproofing paper; lacteal flour for babies; dietary supplements for humans; dietary supplements for human consumption; dietary food supplements; dietetic beverages adapted for medical purposes; dietetic foods adapted for medical purposes; dietetic substances for medical use; dietetic substances adapted for medical use; dietetic food and substances adapted for medical or veterinary use; dietetic food and substances adapted for medical or veterinary use, food for babies; beverages for babies; food for babies; dietary supplements for animals; nutritional supplements for animals; dietary foods supplements for pets; dietary foods supplements for livestock feed; dietary foods supplements for wild animals; dietary foods supplements for sea animals; dietary foods supplements for fish; semen for artificial insemination; propolis dietary supplements. Binding agents for ice cream; meat tenderizers for household purposes; preparations for stiffening whipped cream; aromatic preparations for food, not from essential oils; aromatic preparations for food; aromatic preparations being flavourings for drinks, not from essential oils; aromatic preparations being flavourings for drinks; tea; prepared coffee and coffee-based beverages; coffee; coffee-based beverages; coffee substitutes; prepared cocoa and cocoa-based beverages; cocoa; cocoa-based beverages; confectionery other than fruit-based, vegetable-based, bean-based or nut-based; chocolate desserts, muesli desserts, custard-based desserts, ice cream desserts; cereal-based, chocolate-based and rice-based snacks; confectionery; bread and buns; sandwiches; steamed buns stuffed with minced meat [Chuka-manjuh]; hamburgers [sandwiches]; hamburger sandwiches; pizzas; hot dogs [sandwiches]; hot dogs sandwiches; meat pies; seasonings [other than spices]; seasonings; sauces [condiments]; miso; worcester sauce; meat gravies; ketchup; tomato ketchup; ketchup (sauce); soy sauce [soya sauce]; soy sauce; soya sauce; vinegar; vinegar mixes; vinegar base; seasoning soy sauce [Sobatsuyu]; salad dressings; white sauce; bechamel [white sauce]; mayonnaise; sauces for barbecued meat; barbecue sauce; cube sugar; fructose for culinary purposes; crystal sugar [not confectionery]; sugar; maltose for culinary purposes; maltose; honey; glucose for culinary purposes; powdered starch syrup for culinary purposes; powdered candy; starch syrup for culinary purposes; table salt mixed with sesame seeds; cooking salt; roasted and ground sesame seeds; celery salt; umami seasonings; spices; ice cream mixes; sherbet mixes [ices]; cereal preparations; chocolate spread; chocolate-based spreads; yeast powder; Koji [fermented malted rice]; yeast; baking powder; instant confectionery mixes; pasta sauce; by-product of rice for food [Sake lees]; husked rice; husked oats; husked barley; gluten for food; gluten prepared as foodstuff; flour; propolis; royal jelly. Food processing; processing of foodstuffs for use in manufacture; plant extraction being services of biological materials treatment; animal extraction being services of biological materials treatment; fruit crushing; processing of raw materials for the manufacture of functional foods; custom manufacture of dietary supplements; custom manufacture of dietary supplements for human beings; processing of raw materials for the manufacture of food and beverages; processing of raw materials for the manufacture of cosmetics; processing of chemicals; processing of raw materials for the manufacture of pharmaceuticals; custom manufacture of pharmaceuticals; custom manufacture of products for the pharmaceutical, chemical and food industries by compressing and compacting powders and granules; processing of artificial limbs or artificial teeth, including processing of medical materials; water treating; recycling of waste; rental of machines and apparatus for processing foods or beverages; rental of water purifying apparatus; rental of chemical processing machines and apparatus; providing material treatment information; custom manufacture of pharmaceutical raw materials; custom manufacture of drug substance; custom manufacture of pharmaceutical intermediate; custom manufacture of pharmaceutical additives; custom manufacture of pharmaceutical ingredients; custom manufacture of chemicals; custom manufacture of cosmetics; custom manufacture of cosmetic ingredients; custom processing of foods, other than cooking; custom processing of ingredients for food industry; custom manufacture of medical materials; custom manufacture of amino acids; custom manufacture of active pharmaceutical ingredients; custom manufacture of biopharmaceuticals. Providing meteorological information; architectural design; surveying; geological surveys or research; geological surveys; geological research; designing of machines, apparatus, instruments [including their parts] or systems composed of such machines, apparatus and instruments; designing, other than for advertising purposes; computer software design, computer programming, or maintenance of computer software; computer software design; computer programming; maintenance of computer software; technological advice relating to computers, automobiles and industrial machines; testing, inspection or research of pharmaceuticals, cosmetics or foodstuffs; pharmaceutical research service; pharmaceutical research; medical research; testing, inspection or research of pharmaceutical raw materials; research of pharmaceutical production methods; testing, inspection or research of drug substance; research of drug substance production methods; testing, inspection or research of pharmaceutical intermediate; research of pharmaceutical intermediate production method; testing, inspection or research of pharmaceutical additives; research of pharmaceutical additive production methods; testing, inspection or research of pharmaceutical ingredients; research of pharmaceutical ingredient production methods; testing, inspection or research of chemicals; chemical analysis; chemical research; research of chemical production methods; development and test of chemical production methods; testing, inspection or research of cosmetics; research of cosmetic production methods; laboratory research in the field of cosmetics; laboratory analysis in the field of cosmetics; testing, inspection or research of cosmetic ingredients; research of cosmetic ingredient production methods; testing, inspection or research of foodstuffs; food research; research on food; research in the field of food; research of foodstuff production methods; testing, inspection or research of foodstuff ingredients; research of foodstuff ingredient production methods; testing, inspection or research of medical materials; research of medical material production methods; testing, inspection or research in the field of pharmaceutical, chemical and food industries; research of production methods in the field of pharmaceutical, chemical and food industries; testing, inspection and research services in the fields of pharmaceuticals, cosmetics and foodstuffs; research on building construction or city planning; testing or research on prevention of pollution; testing or research on electricity; testing or research on civil engineering; testing, inspection or research of agriculture, livestock breeding or fisheries; testing or research on machines, apparatus and instruments; rental of measuring apparatus; rental of computers; providing computer programs on data networks; rental of laboratory apparatus and instruments; rental of technical drawing instruments; design and development of new technology for others; scientific research and development; scientific and medical research and development; provision of information and data relating to scientific and technological research and development; research and development of new products for others; product development for others.

3.

HAMARI

      
Application Number 1692804
Status Registered
Filing Date 2022-03-03
Registration Date 2022-03-03
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ?
  • 01 - Chemical and biological materials for industrial, scientific and agricultural use
  • 03 - Cosmetics and toiletries; cleaning, bleaching, polishing and abrasive preparations
  • 05 - Pharmaceutical, veterinary and sanitary products
  • 30 - Basic staples, tea, coffee, baked goods and confectionery
  • 40 - Treatment of materials; recycling, air and water treatment,
  • 42 - Scientific, technological and industrial services, research and design

Goods & Services

Chemicals; industrial chemicals; chemicals used in science; plant extracts for use in the manufacture of pharmaceuticals; plant extracts for use in the manufacture of cosmetics; plant extracts for use in the manufacture of food; chemical additives for use in the manufacture of food; animal extracts for use in manufacture of pharmaceuticals; animal extracts for use in manufacture of cosmetics; animal extracts for use in the manufacture of foods; glues and adhesives for industrial purposes; plant growth regulating preparations; chemicals used in agriculture, horticulture and forestry; fertilizers; ceramic glazings; oil cement [putty]; higher fatty acids; fatty acids for industrial purpose; non-metallic minerals; non-metallic minerals for use in manufacture; photographic chemicals; photographic developers; reagent paper [not for medical purposes]; reagent paper, other than for medical or veterinary purposes; artificial sweeteners; artificial sweeteners [chemical preparations]; flour and starch for industrial purposes; plastics [raw materials]; plastics, unprocessed; paper pulp, cellulose pulp, wood pulp; paper pulp; dissolving pulp. Anti-static preparations for household purposes; de-greasing preparations for household purposes; rust removing preparations; stain removing benzine; fabric softeners for laundry use; laundry bleach; adhesives for affixing false hair; laundry starch; seaweed gelatine for laundry use [Funori]; adhesives for affixing false eyelashes; breath freshening preparations; breath freshening preparations for personal hygiene; deodorants for animals; paint stripping preparations; shoe cream; shoe black [shoe polish]; polishing preparations; soaps and detergents; bar soap; bath soaps; liquid soap; detergent soap; detergents for household use; dentifrices; cosmetics; perfumes and fragrances; perfumes; perfumes for industrial purposes; essential oils for use as food and drink flavorings; essential oils; body deodorant cosmetics and fragrances; fragrances; incense; abrasive paper; abrasive cloth; abrasive sand; artificial pumice stone; polishing paper; false nails; false eyelashes. Pharmaceutical preparations and other preparations for destroying vermin, fungicides, herbicides; pharmaceutical preparations; pharmaceutical, medical and veterinary preparations; chemical reagents for medical or veterinary purposes; vitamin preparations; nutritional additives; disinfectants; preparations for destroying vermin; fungicides; herbicides; plant extracts for pharmaceutical purposes; nutritional supplement drinks; nursing tonic nutritional supplement drinks; nutritional supplement beverage; reagent paper for medical purposes; oiled paper for medical purposes; adhesive tapes for medical purposes; drug delivery agents in the form of edible wafers for wrapping powdered pharmaceuticals; gauze for dressings; empty capsules for pharmaceuticals; eyepatches for medical purposes; ear bandages; menstruation bandages; menstruation tampons; sanitary napkins; sanitary panties; absorbent cotton; adhesive plasters; bandages for dressings; liquid bandages; liquid bandages for skin wounds; breast-nursing pads; cotton swabs for medical use; dental materials; diapers; diaper covers; mothproofing paper; lacteal flour for babies; dietary supplements for humans; dietary supplements for human consumption; dietary food supplements; dietetic beverages adapted for medical purposes; dietetic foods adapted for medical purposes; dietetic substances for medical use; dietetic substances adapted for medical use; dietetic food and substances adapted for medical or veterinary use; dietetic food and substances adapted for medical or veterinary use, food for babies; beverages for babies; food for babies; dietary supplements for animals; nutritional supplements for animals; dietary foods supplements for pets; dietary foods supplements for livestock feed; dietary foods supplements for wild animals; dietary foods supplements for sea animals; dietary foods supplements for fish; semen for artificial insemination; propolis dietary supplements. Binding agents for ice cream; meat tenderizers for household purposes; preparations for stiffening whipped cream; aromatic preparations for food, not from essential oils; aromatic preparations for food; aromatic preparations being flavourings for drinks, not from essential oils; aromatic preparations being flavourings for drinks; tea; prepared coffee and coffee-based beverages; coffee; coffee-based beverages; coffee substitutes; prepared cocoa and cocoa-based beverages; cocoa; cocoa-based beverages; confectionery other than fruit-based, vegetable-based, bean-based or nut-based; chocolate desserts, muesli desserts, custard-based desserts, ice cream desserts; cereal-based, chocolate-based and rice-based snacks; confectionery; bread and buns; sandwiches; steamed buns stuffed with minced meat [Chuka-manjuh]; hamburgers [sandwiches]; hamburger sandwiches; pizzas; hot dogs [sandwiches]; hot dogs sandwiches; meat pies; seasonings [other than spices]; seasonings; sauces [condiments]; miso; worcester sauce; meat gravies; ketchup; tomato ketchup; ketchup (sauce); soy sauce [soya sauce]; soy sauce; soya sauce; vinegar; vinegar mixes; vinegar base; seasoning soy sauce [Sobatsuyu]; salad dressings; white sauce; bechamel [white sauce]; mayonnaise; sauces for barbecued meat; barbecue sauce; cube sugar; fructose for culinary purposes; crystal sugar [not confectionery]; sugar; maltose for culinary purposes; maltose; honey; glucose for culinary purposes; powdered starch syrup for culinary purposes; powdered candy; starch syrup for culinary purposes; table salt mixed with sesame seeds; cooking salt; roasted and ground sesame seeds; celery salt; umami seasonings; spices; ice cream mixes; sherbet mixes [ices]; cereal preparations; chocolate spread; chocolate-based spreads; yeast powder; Koji [fermented malted rice]; yeast; baking powder; instant confectionery mixes; pasta sauce; by-product of rice for food [Sake lees]; husked rice; husked oats; husked barley; gluten for food; gluten prepared as foodstuff; flour; propolis; royal jelly. Food processing; processing of foodstuffs for use in manufacture; plant extraction being services of biological materials treatment; animal extraction being services of biological materials treatment; fruit crushing; processing of raw materials for the manufacture of functional foods; custom manufacture of dietary supplements; custom manufacture of dietary supplements for human beings; processing of raw materials for the manufacture of food and beverages; processing of raw materials for the manufacture of cosmetics; processing of chemicals; processing of raw materials for the manufacture of pharmaceuticals; custom manufacture of pharmaceuticals; custom manufacture of products for the pharmaceutical, chemical and food industries by compressing and compacting powders and granules; processing of artificial limbs or artificial teeth, including processing of medical materials; water treating; recycling of waste; rental of machines and apparatus for processing foods or beverages; rental of water purifying apparatus; rental of chemical processing machines and apparatus; providing material treatment information; custom manufacture of pharmaceutical raw materials; custom manufacture of drug substance; custom manufacture of pharmaceutical intermediate; custom manufacture of pharmaceutical additives; custom manufacture of pharmaceutical ingredients; custom manufacture of chemicals; custom manufacture of cosmetics; custom manufacture of cosmetic ingredients; custom processing of foods, other than cooking; custom processing of ingredients for food industry; custom manufacture of medical materials; custom manufacture of amino acids; custom manufacture of active pharmaceutical ingredients; custom manufacture of biopharmaceuticals. Providing meteorological information; architectural design; surveying; geological surveys or research; geological surveys; geological research; designing of machines, apparatus, instruments [including their parts] or systems composed of such machines, apparatus and instruments; designing, other than for advertising purposes; computer software design, computer programming, or maintenance of computer software; computer software design; computer programming; maintenance of computer software; technological advice relating to computers, automobiles and industrial machines; testing, inspection or research of pharmaceuticals, cosmetics or foodstuffs; pharmaceutical research service; pharmaceutical research; medical research; testing, inspection or research of pharmaceutical raw materials; research of pharmaceutical production methods; testing, inspection or research of drug substance; research of drug substance production methods; testing, inspection or research of pharmaceutical intermediate; research of pharmaceutical intermediate production method; testing, inspection or research of pharmaceutical additives; research of pharmaceutical additive production methods; testing, inspection or research of pharmaceutical ingredients; research of pharmaceutical ingredient production methods; testing, inspection or research of chemicals; chemical analysis; chemical research; research of chemical production methods; development and test of chemical production methods; testing, inspection or research of cosmetics; research of cosmetic production methods; laboratory research in the field of cosmetics; laboratory analysis in the field of cosmetics; testing, inspection or research of cosmetic ingredients; research of cosmetic ingredient production methods; testing, inspection or research of foodstuffs; food research; research on food; research in the field of food; research of foodstuff production methods; testing, inspection or research of foodstuff ingredients; research of foodstuff ingredient production methods; testing, inspection or research of medical materials; research of medical material production methods; testing, inspection or research in the field of pharmaceutical, chemical and food industries; research of production methods in the field of pharmaceutical, chemical and food industries; testing, inspection and research services in the fields of pharmaceuticals, cosmetics and foodstuffs; research on building construction or city planning; testing or research on prevention of pollution; testing or research on electricity; testing or research on civil engineering; testing, inspection or research of agriculture, livestock breeding or fisheries; testing or research on machines, apparatus and instruments; rental of measuring apparatus; rental of computers; providing computer programs on data networks; rental of laboratory apparatus and instruments; rental of technical drawing instruments; design and development of new technology for others; scientific research and development; scientific and medical research and development; provision of information and data relating to scientific and technological research and development; research and development of new products for others; product development for others.

4.

PepZinGi

      
Application Number 1670506
Status Registered
Filing Date 2021-12-01
Registration Date 2021-12-01
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ?
  • 01 - Chemical and biological materials for industrial, scientific and agricultural use
  • 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Chemicals; industrial chemicals. Dietary supplements for humans; dietary supplements for human consumption; dietary food supplements; dietary supplements consisting of minerals; dietetic beverages adapted for medical purposes; dietetic food adapted for medical purposes; dietetic substances for medical use other than pharmaceutical preparations; dietetic substances adapted for medical use other than pharmaceutical preparations; dietetic food and substances adapted for medical or veterinary use other than pharmaceutical preparations; dietetic food and substances adapted for medical or veterinary use, food for babies other than pharmaceutical preparations; beverages for babies; food for babies; dietary supplements for animals; nutritional supplements for animals; dietary food supplements for pets; dietary food supplements for livestock feed; dietary foods supplements for wild animals; dietary food supplements for sea animals; dietary foods supplements for fish.

5.

Tailor-Made Amino Acids

      
Application Number 1667126
Status Registered
Filing Date 2021-12-01
Registration Date 2021-12-01
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ?
  • 01 - Chemical and biological materials for industrial, scientific and agricultural use
  • 40 - Treatment of materials; recycling, air and water treatment,
  • 42 - Scientific, technological and industrial services, research and design

Goods & Services

Chemicals; industrial chemicals; chemical used in science; glue and adhesives for industrial purposes; plant growth regulating preparations; chemical used in agriculture, horticulture and forestry; fertilizers; ceramic glazings; oil cement [putty]; higher fatty acids; fatty acids for industrial purpose; non-metallic minerals; non-metallic minerals for use in manufacture; photographic chemicals; reagent paper [not for medical purposes]; reagent paper, other than for medical or veterinary purposes; artificial sweeteners; flour and starch for industrial purposes; plastics [raw materials]; plastic, unprocessed; pulp; paper pulp; dissolving pulp. Custom manufacture of pharmaceuticals; custom manufacture of products for the pharmaceutical, chemical and food industries by compressing and compacting powders and granules; custom manufacture of pharmaceutical raw materials; custom manufacture of drug substance; custom manufacture of pharmaceutical intermediate; custom manufacture of pharmaceutical additives; custom manufacture of pharmaceutical ingredients; custom manufacture of chemicals; custom manufacture of cosmetics; custom manufacture of cosmetic ingredients; custom manufacture of foods; custom manufacture of food ingredients; custom manufacture of medical materials; custom manufacture of amino acids; custom manufacture of active pharmaceutical ingredients; custom manufacture of biopharmaceuticals. Testing, inspection or research of pharmaceuticals, cosmetics or foodstuffs; pharmaceutical research services; pharmaceutical research; medical research; testing, inspection or research of pharmaceutical raw materials; research of pharmaceutical production methods; testing, inspection or research of drug substance; research of drug substance production methods; testing, inspection or research of pharmaceutical intermediate; research of pharmaceutical intermediate production method; testing, inspection or research of pharmaceutical additives; research of pharmaceutical additive production methods; testing, inspection or research of pharmaceutical ingredients; research of pharmaceutical ingredient production methods; testing, inspection or research of chemicals; chemical analysis; chemical research; research of chemical production methods; development and test of chemical production methods; testing, inspection or research of cosmetics; research of cosmetic production methods; laboratory research in the field of cosmetics; laboratory analysis in the field of cosmetics; testing, inspection or research of cosmetic ingredients; research of cosmetic ingredient production methods; testing, inspection or research of foodstuffs; food research; research on food; research in the field of food; research of foodstuff production methods; testing, inspection or research of foodstuff ingredients; research of foodstuff ingredient production methods; testing, inspection or research of medical materials; research of medical material production methods; testing, inspection or research of pharmaceutical products and foods and drinks; research on manufacturing methods for pharmaceutical products and foods and drinks; testing, inspection or research on agriculture, livestock breeding or fisheries; design and development of new technology for others; scientific research and development; scientific and medical research and development; provision of information and data relating to scientific and technological research and development; research and development of new products for others; product development for others.

6.

PepZinGi

      
Application Number 1654885
Status Registered
Filing Date 2021-12-01
Registration Date 2021-12-01
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ?
  • 01 - Chemical and biological materials for industrial, scientific and agricultural use
  • 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Chemicals; industrial chemicals. Dietary supplements for humans; dietary supplements for human consumption; dietary food supplements; dietary supplements consisting of minerals; dietetic beverages adapted for medical purposes; dietetic food adapted for medical purposes; dietetic substances for medical use other than pharmaceutical preparations; dietetic substances adapted for medical use other than pharmaceutical preparations; dietetic food and substances adapted for medical or veterinary use other than pharmaceutical preparations; dietetic food and substances adapted for medical or veterinary, food for babies other than pharmaceutical preparations; beverages for babies; food for babies; dietary supplements for animals; nutritional supplements for animals; dietary food supplements for pets; dietary food supplements for livestock feed; dietary foods supplements for wild animals; dietary food supplements for sea animals; dietary foods supplements for fish.

7.

Miscellaneous Design

      
Serial Number 79353937
Status Registered
Filing Date 2022-03-03
Registration Date 2024-07-16
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ? 01 - Chemical and biological materials for industrial, scientific and agricultural use

Goods & Services

Industrial chemicals

8.

HAMARI

      
Serial Number 79353938
Status Registered
Filing Date 2022-03-03
Registration Date 2024-02-20
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ? 01 - Chemical and biological materials for industrial, scientific and agricultural use

Goods & Services

Industrial chemicals

9.

PepZinGi

      
Application Number 217753400
Status Pending
Filing Date 2021-12-01
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ?
  • 01 - Chemical and biological materials for industrial, scientific and agricultural use
  • 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

(1) Chemicals; industrial chemicals. (2) Dietary supplements for humans; dietary supplements for human consumption; dietary food supplements; dietary supplements consisting of minerals; dietetic beverages adapted for medical purposes; dietetic food adapted for medical purposes; dietetic substances for medical use other than pharmaceutical preparations; dietetic substances adapted for medical use other than pharmaceutical preparations; dietetic food and substances adapted for medical or veterinary use other than pharmaceutical preparations; dietetic food and substances adapted for medical or veterinary, food for babies other than pharmaceutical preparations; beverages for babies; food for babies; dietary supplements for animals; nutritional supplements for animals; dietary food supplements for pets; dietary food supplements for livestock feed; dietary foods supplements for wild animals; dietary food supplements for sea animals; dietary foods supplements for fish.

10.

PEPZINGI

      
Serial Number 79337723
Status Registered
Filing Date 2021-12-01
Registration Date 2023-01-03
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ?
  • 01 - Chemical and biological materials for industrial, scientific and agricultural use
  • 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Industrial chemicals Dietary food supplements

11.

PEPZINGI

      
Application Number 219615500
Status Pending
Filing Date 2021-12-01
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ?
  • 01 - Chemical and biological materials for industrial, scientific and agricultural use
  • 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

(1) Chemicals; industrial chemicals. (2) Dietary supplements for humans; dietary supplements for human consumption; dietary food supplements; dietary supplements consisting of minerals; dietetic beverages adapted for medical purposes; dietetic food adapted for medical purposes; dietetic substances for medical use other than pharmaceutical preparations; dietetic substances adapted for medical use other than pharmaceutical preparations; dietetic food and substances adapted for medical or veterinary use other than pharmaceutical preparations; dietetic food and substances adapted for medical or veterinary use, food for babies other than pharmaceutical preparations; beverages for babies; food for babies; dietary supplements for animals; nutritional supplements for animals; dietary food supplements for pets; dietary food supplements for livestock feed; dietary foods supplements for wild animals; dietary food supplements for sea animals; dietary foods supplements for fish.

12.

PEPZINGI

      
Serial Number 79344277
Status Registered
Filing Date 2021-12-01
Registration Date 2023-07-11
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ?
  • 01 - Chemical and biological materials for industrial, scientific and agricultural use
  • 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Industrial chemicals Dietary food supplements

13.

Method for producing peptide

      
Application Number 16496245
Grant Number 11084846
Status In Force
Filing Date 2018-03-29
First Publication Date 2020-01-23
Grant Date 2021-08-10
Owner Hamari Chemicals, Ltd. (Japan)
Inventor
  • Sumino, Fumitoshi
  • Deguchi, Ayaka
  • Ono, Rui
  • Hiroyama, Yuta
  • Kanno, Teruhiko
  • Moriwaki, Hiroki

Abstract

An object of the present invention is to provide a novel solid phase peptide synthesis method for synthesizing a large amount of a peptide. Another object of the present invention is to provide a novel solid phase peptide synthesis method for synthesizing a high-purity long-chain peptide. Still another object of the present invention is to provide a novel solid phase peptide synthesis method causing fewer side reactions. The present invention relates to a method for producing a peptide, and the method comprises solid-phase synthesis of a peptide under stirring with a centrifugal stirrer having no impeller.

IPC Classes  ?

  • C07K 1/04 - General processes for the preparation of peptides on carriers
  • B01J 8/10 - Chemical or physical processes in general, conducted in the presence of fluids and solid particlesApparatus for such processes with moving particles moved by stirrers or by rotary drums or rotary receptacles
  • B01F 7/32 - Mixers with rotary stirring devices in fixed receptacles; Kneaders with stirrers rotating about a vertical axis with openwork frames or cages
  • B01F 15/06 - Heating or cooling systems
  • C07K 1/34 - ExtractionSeparationPurification by filtration, ultrafiltration or reverse osmosis
  • B01J 19/00 - Chemical, physical or physico-chemical processes in generalTheir relevant apparatus

14.

METHOD FOR PRODUCING PEPTIDE

      
Application Number JP2018013147
Publication Number 2018/181679
Status In Force
Filing Date 2018-03-29
Publication Date 2018-10-04
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Sumino, Fumitoshi
  • Deguchi, Ayaka
  • Ono, Rui
  • Hiroyama, Yuta
  • Kanno, Teruhiko
  • Moriwaki, Hiroki

Abstract

The present invention addresses the problem of providing a novel peptide solid-phase synthesis method for synthesizing a peptide in a large quantity. The present invention also addresses the problem of providing a novel peptide solid-phase synthesis method for synthesizing a long-chain peptide having high purity. The present invention also addresses the problem of providing a novel peptide solid-phase synthesis method which causes few side reactions. The present invention relates to a method for producing a peptide, characterized in that the peptide is solid-phase-synthesized while stirring with a centrifugal stirrer equipped with no impeller.

IPC Classes  ?

  • C07K 1/04 - General processes for the preparation of peptides on carriers
  • B01F 7/16 - Mixers with rotary stirring devices in fixed receptacles; Kneaders with stirrers rotating about a vertical axis
  • B01F 7/32 - Mixers with rotary stirring devices in fixed receptacles; Kneaders with stirrers rotating about a vertical axis with openwork frames or cages
  • C07K 1/34 - ExtractionSeparationPurification by filtration, ultrafiltration or reverse osmosis

15.

Axially chiral N-(2-acylaryl)-2-[5,7-dihydro-6h-dibenzo[c,e]azepin-6-yl] acetamide compound and chirality interconversion method of a-amino acid using the same

      
Application Number 14651857
Grant Number 09688612
Status In Force
Filing Date 2013-12-17
First Publication Date 2015-11-12
Grant Date 2017-06-27
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Moriwaki, Hiroki
  • Takeda, Ryosuke
  • Kawamura, Akie
  • Kawashima, Aki
  • Soloshonok, Vadim A.

Abstract

An object of the present invention is to provide a method for producing an optically active amino acid in high yield and in a highly enantioselective manner, which method has fewer restrictions on the material that can be used as the substrate, and to provide, among others, a compound useful as a chiral auxiliary for the method. The present invention provides an N-(2-acylaryl)-2-[5,7-dihydro-6H-dibenzo[c,e]azepin-6-yl]acetamide compound represented by Formula (1): or a salt thereof, or a metal complex represented, by Formula (3):

IPC Classes  ?

  • C07D 223/14 - Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
  • C07D 223/18 - DibenzazepinesHydrogenated dibenzazepines
  • C07C 227/30 - Preparation of optical isomers
  • C07C 319/12 - Preparation of thiols, sulfides, hydropolysulfides or polysulfides of thiols by reactions not involving the formation of mercapto groups
  • C07D 209/20 - Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
  • C07B 53/00 - Asymmetric syntheses
  • C07C 227/32 - Preparation of optical isomers by stereospecific synthesis
  • C07C 229/08 - Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to hydrogen atoms
  • C07C 229/36 - Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings with at least one amino group and one carboxyl group bound to the same carbon atom of the carbon skeleton
  • C07F 15/04 - Nickel compounds

16.

METHOD FOR SYNTHESIZING OPTICALLY ACTIVE α-AMINO ACID USING CHIRAL METAL COMPLEX COMPRISING AXIALLY CHIRAL N-(2-ACYLARYL)-2-[5,7-DIHYDRO-6H-DIBENZO[c,e]AZEPIN-6-YL]ACETAMIDE COMPOUND AND AMINO ACID

      
Application Number JP2014058974
Publication Number 2014/188783
Status In Force
Filing Date 2014-03-27
Publication Date 2014-11-27
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Moriwaki, Hiroki
  • Kawashima, Aki
  • Takeda, Ryosuke
  • Kawamura, Akie
  • Soloshonok Vadim A.

Abstract

 The purpose of the invention is to provide a production method that makes possible the industrial production of an optically active α-amino acid at high yield and high enantioselectivity, to provide a simple method for producing optically active α,α-disubstituted α-amino acid, and to provide an intermediate useful in the methods for producing the above optically active α-amino acid and α,α-disubstituted α-amino acid. Provided is a method for producing an optically active α-amino acid or salt thereof characterized in that a substituent is introduced at the α carbon of the α-amino acid moiety structure of a metal complex represented by formula (1) by an alkylation reaction, Aldol reaction, Michael reaction, or Mannich reaction, and an optically pure α-amino acid enantiomer or salt thereof is then liberated by decomposing the metal complex by an acid.

IPC Classes  ?

  • C07F 15/04 - Nickel compounds
  • C07C 227/32 - Preparation of optical isomers by stereospecific synthesis
  • C07C 229/24 - Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having more than one carboxyl group bound to the carbon skeleton, e.g. aspartic acid
  • C07C 229/30 - Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and unsaturated
  • C07C 229/36 - Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings with at least one amino group and one carboxyl group bound to the same carbon atom of the carbon skeleton
  • C07C 229/48 - Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups and carboxyl groups bound to carbon atoms of the same non-condensed ring
  • C07C 231/18 - Preparation of optical isomers by stereospecific synthesis
  • C07C 237/06 - Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
  • C07C 319/20 - Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides by reactions not involving the formation of sulfide groups
  • C07C 323/58 - Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups with amino groups bound to the carbon skeleton
  • C07D 213/55 - AcidsEsters
  • C07D 223/14 - Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
  • C07B 53/00 - Asymmetric syntheses

17.

Method for producing optically active alcohols

      
Application Number 14353484
Grant Number 09174899
Status In Force
Filing Date 2012-10-24
First Publication Date 2014-10-02
Grant Date 2015-11-03
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Maeda, Sadayuki
  • Sato, Tatsunori

Abstract

A method is provided for producing optically active alcohols from ketones by reducing a ketone in the presence of an iridium(III) complex having a chiral prolinamide compound as a ligand. The ketone is preferably a compound represented by formula [I]: 2 may be bound to each other at any appropriate position to form a ring, the ring optionally containing one or more atoms which may be the same or different and are selected from an oxygen atom, an optionally substituted nitrogen atom and a sulfur atom, and optionally being condensed with an aromatic or hetero-aromatic ring).

IPC Classes  ?

  • C07D 207/09 - Radicals substituted by nitrogen atoms not forming part of a nitro radical
  • C07C 29/143 - Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen-containing functional group of C=O containing groups, e.g. —COOH of ketones
  • C07D 311/74 - Benzo [b] pyrans, hydrogenated in the carbocyclic ring
  • C07C 41/26 - Preparation of ethers by reactions not forming ether-oxygen bonds by introduction of hydroxy or O-metal groups
  • C07B 53/00 - Asymmetric syntheses

18.

Method for producing optically active tetrahydroquinolines

      
Application Number 14232589
Grant Number 09108986
Status In Force
Filing Date 2012-07-13
First Publication Date 2014-08-14
Grant Date 2015-08-18
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Maeda, Sadayuki
  • Sato, Tatsunori
  • Kawano, Yasuhiko
  • Miyawaki, Toshio

Abstract

Provided are a novel chiral iridium(III) complex; and a method for producing optically active 2-substituted-1,2,3,4-tetrahydroquinolines from 2-substituted-quinolines with the use of the chiral iridium(III) complex through a more economical and easy production process. The disclosed method for producing optically active 2-substituted-1,2,3,4-tetrahydroquinolines comprises reducing a quinoline compound represented by formula [I]: in the presence of a hydrogen donor compound and an iridium (III) complex having a chiral prolinamide compound as a ligand to give an optically active 2-substituted-1,2,3,4-tetrahydroquinoline represented by formula [II]:

IPC Classes  ?

  • C07D 215/00 - Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
  • C07F 5/00 - Compounds containing elements of Groups 3 or 13 of the Periodic Table
  • C07D 215/04 - Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms
  • C07B 53/00 - Asymmetric syntheses
  • C07F 17/02 - Metallocenes of metals of Groups 8, 9 or 10 of the Periodic Table
  • C07D 215/06 - Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms having only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to the ring nitrogen atom
  • C07D 215/18 - Halogen atoms or nitro radicals
  • C07D 215/20 - Oxygen atoms
  • C07D 215/22 - Oxygen atoms attached in position 2 or 4
  • C07D 215/227 - Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
  • C07D 215/14 - Radicals substituted by oxygen atoms

19.

AXIALLY CHIRAL N-(2-ACYLARYL)-2-[5,7-DIHYDRO-6H-DIBENZO[C,E]AZEPIN-6-YL]ACETAMIDE COMPOUND AND CHIRALITY INTERCONVERSION METHOD OF .ALPHA.-AMINO ACID USING THE SAME

      
Document Number 02895334
Status In Force
Filing Date 2013-12-17
Open to Public Date 2014-06-26
Grant Date 2020-12-29
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Moriwaki, Hiroki
  • Takeda, Ryosuke
  • Kawamura, Akie
  • Kawashima, Aki
  • Soloshonok Vadim A.,

Abstract

An object of the present invention is to provide a method for producing an optically active amino acid in high yield and in a highly enantioselective manner, which method has fewer restrictions on the material that can be used as the substrate, and to provide, among others, a compound useful as a chiral auxiliary for the method. The present invention provides an N-(2-acylaryl)-2-[5,7-dihydro-6H-dibenzo[c,e]azepin-6-yl]acetamide compound represented by Formula (1):(See Formula 1)or a salt thereof, or a metal complex represented by Formula (3):(See Formula 3)

IPC Classes  ?

  • C07B 53/00 - Asymmetric syntheses
  • C07B 61/00 - Other general methods
  • C07C 227/32 - Preparation of optical isomers by stereospecific synthesis
  • C07C 229/08 - Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to hydrogen atoms
  • C07C 229/36 - Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings with at least one amino group and one carboxyl group bound to the same carbon atom of the carbon skeleton
  • C07D 223/14 - Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
  • C07F 15/04 - Nickel compounds

20.

AXIAL-ASYMMETRIC N-(2-ACYLARYL)-2-[5, 7-DIHYDRO-6H-DIBENZO [C, E] AZEPINE-6-YL] ACETAMIDE COMPOUND AND CHIRALITY CONVERSION METHOD FOR Α-AMINO ACID USING SAME

      
Application Number JP2013083711
Publication Number 2014/098063
Status In Force
Filing Date 2013-12-17
Publication Date 2014-06-26
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Moriwaki, Hiroki
  • Takeda, Ryosuke
  • Kawamura, Akie
  • Kawashima, Aki
  • Soloshonok Vadim A.

Abstract

The present invention addresses the problem of providing: a production method capable of high-yield/high-enantioselectively producing an optically active amino acid having few restrictions on the material that can be used as the substrate therefor; and a useful compound, as a chiral auxiliary agent; etc. The present invention provides an N-(2-acylaryl)-2-[5, 7-dihydro-6H-dibenzo [c, e] azepine-6-yl] acetamide compound indicated in formula (1), a salt thereof, or a metal complex indicated in formula (3).

IPC Classes  ?

  • C07D 223/14 - Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
  • C07C 227/32 - Preparation of optical isomers by stereospecific synthesis
  • C07C 229/08 - Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to hydrogen atoms
  • C07C 229/36 - Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings with at least one amino group and one carboxyl group bound to the same carbon atom of the carbon skeleton
  • C07B 53/00 - Asymmetric syntheses
  • C07B 61/00 - Other general methods
  • C07F 15/04 - Nickel compounds

21.

METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL

      
Application Number JP2012077464
Publication Number 2013/061999
Status In Force
Filing Date 2012-10-24
Publication Date 2013-05-02
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Maeda, Sadayuki
  • Sato, Tatsunori

Abstract

Provided is a method for producing an optically active alcohol with high yield by an industrially advantageous process with use of a low-cost asymmetric catalyst, while using a ketone, which may have various structures, as a starting material. A method for producing an optically active alcohol of the present invention is characterized by reducing a ketone in the presence of an iridium (III) complex that has a chiral proline amide compound as a ligand. It is preferable that the ketone is a compound represented by formula [I]. (In the formula, R1 and R2 are different from each other and represent an optionally substituted linear or branched alkyl group, an optionally substituted cycloalkyl group, an optionally substituted aryl group, an optionally substituted heteroaryl group, an optionally substituted aralkyl group, an optionally substituted heteroaryl alkyl group, an optionally substituted alkenyl group or an optionally substituted alkynyl group; the R1 and R2 may combine together at arbitrary positions to form ring(s); and the rings may be the same or different and contain one or more oxygen atoms, an optionally substituted nitrogen atom or a sulfur atom, and may be fused with an aromatic ring or a heterocyclic aromatic ring.)

IPC Classes  ?

  • C07C 29/143 - Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen-containing functional group of C=O containing groups, e.g. —COOH of ketones
  • C07C 35/17 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic containing six-membered rings with unsaturation only outside the ring
  • C07C 35/22 - Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system
  • C07C 41/26 - Preparation of ethers by reactions not forming ether-oxygen bonds by introduction of hydroxy or O-metal groups
  • C07C 43/196 - Ethers having an ether-oxygen atom bound to a carbon atom of a ring other than a six-membered aromatic ring containing hydroxy or O-metal groups
  • C07D 311/74 - Benzo [b] pyrans, hydrogenated in the carbocyclic ring
  • C07B 53/00 - Asymmetric syntheses
  • C07B 61/00 - Other general methods

22.

METHOD FOR PRODUCING OPTICALLY ACTIVE TETRAHYDROQUINOLINE

      
Application Number JP2012067879
Publication Number 2013/011930
Status In Force
Filing Date 2012-07-13
Publication Date 2013-01-24
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Maeda, Sadayuki
  • Sato, Tatsunori
  • Kawano, Yasuhiko
  • Miyawaki, Toshio

Abstract

Provided are: a novel iridium (III) complex that is chiral; and a production method wherein a 2-substituted-quinoline is converted into an optically active 2-substituted-1,2,3,4-tetrahydroquinoline with use of a chiral iridium (III) complex by economical and easily operable processes. A method for producing an optically active 2-substituted-1,2,3,4-tetrahydroquinoline represented by formula [II], which is characterized by reducing a quinoline compound represented by formula [I] in the presence of a hydrogen-donating compound and an iridium (III) complex that has a chiral proline amide compound as a ligand.

IPC Classes  ?

  • C07D 215/04 - Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms
  • B01J 31/22 - Organic complexes
  • C07B 53/00 - Asymmetric syntheses
  • C07B 61/00 - Other general methods
  • C07F 15/00 - Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
  • C07F 17/00 - Metallocenes

23.

METHOD FOR PRODUCING FINE POWDER OF LOXOPROFEN SODIUM DIHYDRATE FOR PHARMACEUTICAL PREPARATIONS

      
Application Number JP2012058402
Publication Number 2012/137667
Status In Force
Filing Date 2012-03-29
Publication Date 2012-10-11
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Furuyama, Masahiro
  • Yoshida, Kokichi

Abstract

A method for producing a fine powder of loxoprofen sodium dihydrate for pharmaceutical preparations, said method comprising milling loxoprofen sodium dihydrate crystals or a crystalline powder of loxoprofen sodium dihydrate with an impact mill, preferably a pulverizer-type mill, which is provided with a built-in air-classifying system and comprises a pin hammer, to thereby continuously produce a fine powder of loxoprofen sodium dihydrate the volume-average particle size of which is in the range of 20-120 μm, when measured with a laser diffraction particle size analyzer.

IPC Classes  ?

  • A61K 31/192 - Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
  • A61K 9/14 - Particulate form, e.g. powders
  • A61K 9/20 - Pills, lozenges or tablets
  • B02C 13/22 - Disintegrating by mills having rotary beater elements with intermeshing pins

24.

PROPHYLACTIC OR THERAPEUTIC AGENT FOR HYPERLIPEMIA, AND ANTI-FATIGUE AGENT

      
Application Number JP2010073088
Publication Number 2011/078204
Status In Force
Filing Date 2010-12-22
Publication Date 2011-06-30
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Shimazu, Masaji
  • Yazawa, Kazunaga

Abstract

Disclosed are: a prophylactic or therapeutic agent for hyperlipemia, which contains a carnosinase inhibitor and L-carnosines; and an anti-fatigue agent which contains a carnosinase inhibitor and L-carnosines. The free fatty acid concentration in the plasma of a mammal can be decreased by the combined use of a carnosinase inhibitor and L-carnosines. In addition, the lactic acid concentration in the plasma can be decreased by the combined use of a carnosinase inhibitor and L-carnosines, thereby reducing fatigue, enhancing recovery from fatigue and improving endurance. Preferable examples of the carnosinase inhibitor may include β-alanine, N-alkanoyl-β-alanine derivatives, N-alkanoyl-L-carnosine derivatives and the like, and preferable examples of the L-carnosines may include L-carnosine, N-acetyl-L-carnosine, L-anserine, N-acetyl-L-anserine, L-balenine, L-homocarnosine, N-acetyl-L-homocarnosine, carcinine and the like.

IPC Classes  ?

  • A61K 31/4172 - Imidazole-alkanecarboxylic acids, e.g. histidine
  • A61K 31/197 - Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
  • A61K 45/00 - Medicinal preparations containing active ingredients not provided for in groups
  • A61K 47/26 - Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharidesDerivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
  • A61K 47/32 - Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers
  • A61K 47/36 - PolysaccharidesDerivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
  • A61K 47/38 - CelluloseDerivatives thereof
  • A61K 47/42 - ProteinsPolypeptidesDegradation products thereofDerivatives thereof, e.g. albumin, gelatin or zein
  • A61P 1/16 - Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
  • A61P 3/04 - AnorexiantsAntiobesity agents
  • A61P 3/06 - Antihyperlipidemics
  • A61P 3/10 - Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
  • A61P 9/00 - Drugs for disorders of the cardiovascular system
  • A61P 9/04 - Inotropic agents, i.e. stimulants of cardiac contractionDrugs for heart failure
  • A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
  • A61P 9/12 - Antihypertensives
  • A61P 43/00 - Drugs for specific purposes, not provided for in groups

25.

Method for producing optically active amines

      
Application Number 12452402
Grant Number 08222452
Status In Force
Filing Date 2008-06-30
First Publication Date 2010-06-24
Grant Date 2012-07-17
Owner Hamari Chemicals, Ltd. (Japan)
Inventor Maeda, Sadayuki

Abstract

The present invention provides a method for producing chiral amines, comprising asymmetric transfer hydrogenation of imine compounds in the presence of a hydrogen donor compound and an iridium(III) complex having a chiral prolinamide compound as a ligand. The present invention is useful for production of chiral amines in an efficient manner in terms of their optical and chemical yields.

IPC Classes  ?

  • C07C 303/00 - Preparation of esters or amides of sulfuric acidsPreparation of sulfonic acids or of their esters, halides, anhydrides or amides
  • C07C 211/00 - Compounds containing amino groups bound to a carbon skeleton

26.

NOVEL DIHYDROTRIAZINE DERIVATIVE

      
Application Number JP2009064739
Publication Number 2010/024225
Status In Force
Filing Date 2009-08-24
Publication Date 2010-03-04
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Maeda, Shirou
  • Maeda, Akihisa

Abstract

A compound represented by general formula (1), a tautomer thereof, or a salt of the compound or tautomer, which is useful as a bactericide/disinfectant. (In the formula, R1 represents a hydrogen atom, an optionally substituted alkyl group or the like, R2 represents a hydrogen atom or an optionally substituted alkyl group, or alternatively R1 and R2 may combine together with an adjacent nitrogen atom to form an optionally substituted nitrogen-containing heterocyclic group; R4 represents a hydrogen atom or an optionally substituted alkyl group; R3 represents an optionally substituted alkyl group; and R5 and R6 each represents a hydrogen atom or a methyl group.  In this connection, a compound wherein both R2 and R4 represent a hydrogen atom and a compound wherein both R1 and R4 represent a hydrogen atom are excluded.)

IPC Classes  ?

  • C07D 251/10 - Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
  • A61K 8/43 - Guanidines
  • A61K 8/49 - Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
  • A61K 31/155 - Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (HN=C(OH)NH2), isothiourea (HN=C(SH)—NH2)
  • A61K 31/53 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
  • A61P 31/02 - Local antiseptics
  • A61P 31/04 - Antibacterial agents
  • C07C 279/26 - X and Y being nitrogen atoms, i.e. biguanides

27.

PROCESS FOR PRODUCTION OF ETHYNYLTHYMIDINE COMPOUND USING 5-METHYLURIDINE AS STARTING RAW MATERIAL

      
Application Number JP2009057362
Publication Number 2009/125841
Status In Force
Filing Date 2009-04-10
Publication Date 2009-10-15
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Sato, Tatsunori
  • Kawashima, Tetsuya
  • Miwa, Toshio
  • Dokei, Kazutomo
  • Fujimoto, Chikoto

Abstract

Disclosed is a process for producing 2',3'-didehydro-3'-deoxy-4'-ethynylthymidine, which is a compound useful as a pharmaceutical agent, with high efficiency and in an industrially advantageous manner. Specifically disclosed is a process for producing 2',3'-didehydro-3'-deoxy-4'-ethynylthymidine, which is represented by scheme (I). [In the scheme, R1 and R2 independently represent a protective group for a hydroxy group, or R1 and R2 together form a protective group for a hydroxy group; R3 and R4 independently represent a protective group for a hydroxy group; R5 represents a protective group for a hydroxy group; R6 represents a protective group for a hydroxy group; X represents a leaving group; and Y represents a halogen atom.]

IPC Classes  ?

  • C07D 405/04 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring- member bond
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • A61P 31/18 - Antivirals for RNA viruses for HIV
  • A61P 37/04 - Immunostimulants
  • A61P 43/00 - Drugs for specific purposes, not provided for in groups
  • C07H 19/067 - Pyrimidine radicals with ribosyl as the saccharide radical

28.

METHOD FOR PURIFYING ETHYNYLTHYMIDINE COMPOUND

      
Application Number JP2009056219
Publication Number 2009/119785
Status In Force
Filing Date 2009-03-27
Publication Date 2009-10-01
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor
  • Miwa, Toshio
  • Sato, Tatsunori

Abstract

Disclosed is a method for purifying 2',3'-didehydro-3'-deoxy-4'-ethynylthymidine or a base salt thereof, which is characterized in that a crystal of 2',3'-didehydro-3'-deoxy-4'-ethynylthymidine or a base salt thereof is deposited by bringing a solution containing a base salt of 2',3'-didehydro-3'-deoxy-4'-ethynylthymidine and a base salt of a diastereomer of 2',3'-didehydro-3'-deoxy-4'-ethynylthymidine into contact with a solvent in which base salts of 2',3'-didehydro-3'-deoxy-4'-ethynylthymidine are poorly soluble. The method can efficiently and commercially advantageously purify 2',3'-didehydro-3'-deoxy-4'-ethynylthymidine or a base salt thereof, which is useful as a pharmaceutical product.

IPC Classes  ?

  • C07D 405/04 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring- member bond
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
  • A61P 31/18 - Antivirals for RNA viruses for HIV
  • A61P 37/04 - Immunostimulants
  • A61P 43/00 - Drugs for specific purposes, not provided for in groups
  • C07H 19/073 - Pyrimidine radicals with 2-deoxyribosyl as the saccharide radical

29.

METHOD FOR PRODUCING OPTICALLY ACTIVE AMINE

      
Application Number JP2008061809
Publication Number 2009/005024
Status In Force
Filing Date 2008-06-30
Publication Date 2009-01-08
Owner HAMARI CHEMICALS, LTD. (Japan)
Inventor Maeda, Sadayuki

Abstract

Disclosed is a method for producing a chiral amine, which is characterized in that an imine compound is subjected to a hydrogen transfer-type asymmetric reduction in the presence of an iridium (III) complex having a chiral proline amide compound as a ligand and a hydrogen-donating compound. This method is useful for producing a chiral amine efficiently in both optical yield and chemical yield.

IPC Classes  ?

  • C07C 213/02 - Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups
  • C07C 217/70 - Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by singly-bound oxygen atoms with singly-bound oxygen atoms and six-membered aromatic rings bound to the same carbon atom of the carbon chain linked by carbon chains having two carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
  • C07C 303/40 - Preparation of esters or amides of sulfuric acidsPreparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
  • C07C 311/37 - Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
  • C07D 405/04 - Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring- member bond
  • C07B 53/00 - Asymmetric syntheses

30.

BENFOPURE

      
Serial Number 78716411
Status Registered
Filing Date 2005-09-20
Registration Date 2007-04-10
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Food supplements

31.

PEPZINGI

      
Serial Number 78217472
Status Registered
Filing Date 2003-02-21
Registration Date 2004-08-17
Owner HAMARI CHEMICALS, LTD. (Japan)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Mineral food supplements, not for medical purposes

32.

PEPZINGI

      
Application Number 116641000
Status Registered
Filing Date 2003-01-30
Registration Date 2004-04-07
Owner Hamari Chemicals, Ltd. (Japan)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

(1) Mineral food-supplements, not for medical purposes.