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30299-08-2

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30299-08-2 Usage

Description

Clinofibrate, a white solid, is a medication primarily known for its antilipemic properties. It is a member of the fibrate class of drugs, which are used to treat high levels of lipids in the blood. By reducing the levels of low-density lipoprotein (LDL) and very low-density lipoprotein (VLDL), Clinofibrate helps in the management and prevention of atherosclerosis, a condition characterized by the hardening and narrowing of arteries.

Uses

Used in Pharmaceutical Industry:
Clinofibrate is used as an anti-atherosclerosis agent for its ability to lower lipid levels in the blood. This application is particularly important in the treatment and prevention of cardiovascular diseases, as high lipid levels are a significant risk factor for atherosclerosis and related conditions.
Clinofibrate is used as an antilipemic agent for reducing the levels of LDL and VLDL in the blood, which helps in the prevention and management of atherosclerosis and its associated health risks.

Originator

Lipocrin,Sumitomo,Japan,1981

Manufacturing Process

Into a mixture of 6.0 g of a bishydroxyphenyl derivative, and 44.0 g of methyl ethyl ketone was added 16.2 g of crushed potassium hydroxide or sodium hydroxide. Chloroform was added dropwise into the above mixture with stirring at 20°C to 80°C, and the resultant mixture was heated for 20 hours under reflux to complete the reaction. Thereafter the reaction mixture was concentrated to give a residue. Into the residue was added water. After cooling, the resultant mixture was treated with activated charcoal and acidified by diluted hydrochloric acid or sulfuric acid to give an oily substance. The oily substance was extracted by ether and the ether solution was contacted with aqueous diluted Na2CO3 solution. The separated aqueous layer was washed with ether, acidified and again extracted with ether. The obtained ester layer was dried over anhydrous sodium sulfate and concentrated to give 1.0 g of a crude product which was purified by recrystallization or chromatography, to give crystals MP 143°C to 146°C (decomp.)

Check Digit Verification of cas no

The CAS Registry Mumber 30299-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,2,9 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30299-08:
(7*3)+(6*0)+(5*2)+(4*9)+(3*9)+(2*0)+(1*8)=102
102 % 10 = 2
So 30299-08-2 is a valid CAS Registry Number.
InChI:InChI=1/C28H36O6/c1-5-26(3,24(29)30)33-22-14-10-20(11-15-22)28(18-8-7-9-19-28)21-12-16-23(17-13-21)34-27(4,6-2)25(31)32/h10-17H,5-9,18-19H2,1-4H3,(H,29,30)(H,31,32)

30299-08-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (C3100)  Clinofibrate  >98.0%(HPLC)

  • 30299-08-2

  • 200mg

  • 990.00CNY

  • Detail
  • TCI America

  • (C3100)  Clinofibrate  >98.0%(HPLC)

  • 30299-08-2

  • 1g

  • 4,350.00CNY

  • Detail

30299-08-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Clinofibrate

1.2 Other means of identification

Product number -
Other names 2-[4-[1-[4-(2-carboxybutan-2-yloxy)phenyl]cyclohexyl]phenoxy]-2-methylbutanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:30299-08-2 SDS

30299-08-2Relevant articles and documents

Method for preparing high-purity kerley Bette

-

, (2016/10/07)

The invention relates to a preparation method of high-purity clinofibrate, the field of preparation of pharmaceutical compounds. The preparation method comprises the following steps: reacting cyclohexanone and phenol in concentrated hydrochloric acid and glacial acetic acid in a volume ratio of 3:1-7:1 to obtain an intermediate I crude product, decolorizing with a single solvent, and cooling to crystallize to obtain an intermediate I; reacting 2-methylbutyric acid with liquid bromine in phosphorus trichloride, reacting with anhydrous alcohol, extracting, and carrying out vacuum distillation to obtain an intermediate II; reacting the intermediate I and the intermediate II under solventless conditions to obtain an intermediate III; and hydrolyzing the intermediate III and sodium hydroxide, extracting, crystallizing to obtain a clinofibrate crude product; and recrystallizing with an anhydrous solvent to obtain the clinofibrate. The material proportion is adjusted to shorten the production operation period; the invention has the advantages of low energy consumption and low solvent consumption; and the obtained product has the advantages of uniform crystal grains, high purity and low cost.

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