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86227-47-6

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  • Ethyl all cis-5,8,11,14,17-Eicosapentaenoate/Ethyl Icosapentate

    Cas No: 86227-47-6

  • USD $ 95.0-100.0 / Kilogram

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86227-47-6 Usage

Description

ALL CIS-5,8,11,14,17-EICOSAPENTAENOIC ACID ETHYL ESTER, also known as Eicosapentaenoic Acid Ethyl Ester, is a long-chain fatty acid ethyl ester derived from the formal condensation of the carboxy group of (5Z,8Z,11Z,14Z,17Z)-icosapentaenoic acid with the hydroxy group of ethanol. It is an important polyunsaturated fatty acid of the marine food chain and serves as a precursor for the prostaglandin-3 and thromboxane-3 families. It is characterized by its clear colorless oil appearance and is known for its hypolipidemic and antilipemic properties.

Uses

Used in Pharmaceutical Industry:
ALL CIS-5,8,11,14,17-EICOSAPENTAENOIC ACID ETHYL ESTER is used as a hypolipidemic agent for reducing blood lipid levels, which helps in the management of conditions such as hyperlipidemia and atherosclerosis.
Used in Nutritional Supplements:
ALL CIS-5,8,11,14,17-EICOSAPENTAENOIC ACID ETHYL ESTER is used as a nutritional supplement to support heart health and maintain a balanced lipid profile.
Used in Marine Food Chain:
ALL CIS-5,8,11,14,17-EICOSAPENTAENOIC ACID ETHYL ESTER is used as a precursor for the prostaglandin-3 and thromboxane-3 families, playing a crucial role in the marine food chain and contributing to the overall health and well-being of marine organisms.
Brand Name:
Omacor (Reliant) is a brand name under which ALL CIS-5,8,11,14,17-EICOSAPENTAENOIC ACID ETHYL ESTER is marketed, making it easily recognizable and accessible for consumers seeking its health benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 86227-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,2 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86227-47:
(7*8)+(6*6)+(5*2)+(4*2)+(3*7)+(2*4)+(1*7)=146
146 % 10 = 6
So 86227-47-6 is a valid CAS Registry Number.
InChI:InChI=1/C22H34O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24-4-2/h5-6,8-9,11-12,14-15,17-18H,3-4,7,10,13,16,19-21H2,1-2H3/b6-5+,9-8+,12-11+,15-14+,18-17+

86227-47-6 Well-known Company Product Price

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  • TCI America

  • (E0442)  Ethyl all cis-5,8,11,14,17-Eicosapentaenoate  >96.0%(GC)

  • 86227-47-6

  • 200mg

  • 2,450.00CNY

  • Detail
  • TCI America

  • (E0853)  Ethyl all cis-5,8,11,14,17-Eicosapentaenoate (stabilized with Tocopherols)  >65.0%(GC)

  • 86227-47-6

  • 25g

  • 880.00CNY

  • Detail
  • USP

  • (1234307)  Eicosapentaenoic acid ethyl ester  United States Pharmacopeia (USP) Reference Standard

  • 86227-47-6

  • 1234307-500MG

  • 12,636.00CNY

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86227-47-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (5Z,8Z,11Z,14Z,17Z)-icosapentaenoate

1.2 Other means of identification

Product number -
Other names Eicosapentaenoic Acid ethyl este

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:86227-47-6 SDS

86227-47-6Relevant articles and documents

Preparation of n-3 PUFAs ethyl esters by an efficient biocatalyzed solvent-free process

Morrone,D'Antona,Biondi,Lambusta,Nicolosi

, p. 173 - 176 (2012/11/06)

alpha-Linolenic acid (ALA), eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) have been subjected to esterification with ethanol in presence of lipase B from Candida antarctica (Novozym 435), in solvent free condition. The use of alcohol donors triethyl orthoformate (TEOF) or diethyl carbonate (DEC) instead of free ethanol, allowed working in irreversible esterification conditions and ALA-, EPA- and DHA-ethyl esters were obtained in quantitative yields.

Process for the preparation of a composition comprising unsaturated compounds

-

Page/Page column 5, (2008/06/13)

The present invention relates to a process for the preparation of a composition comprising unsaturated compounds, in particular polyunsaturated compounds, which comprises concentrating and purifying the compounds by contact with silicon and/or aluminium derivatives. The process of the invention represents an advantageous substitute of the usual distillation processes, coupled or not to chromatographic processes, and allows to isolate and remove polar byproducts.

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