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73097-00-4

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73097-00-4 Usage

Description

Methyl stearidonate is a compound that can be isolated from the diatom Navicula delognei. It is known for its antibacterial properties, making it a valuable substance in various applications.

Uses

Used in Pharmaceutical Industry:
Methyl stearidonate is used as an antibacterial agent for its ability to inhibit the growth of various harmful bacteria, such as Staphylococcus aureus, S. epidermidis, Salmonella typhimurium, and Proteus vulgaris. This makes it a promising candidate for the development of new antibiotics and treatments for bacterial infections.
Used in Cosmetics Industry:
Methyl stearidonate can also be used as a preservative in the cosmetics industry due to its antibacterial properties. It helps maintain the freshness and safety of cosmetic products by preventing the growth of harmful bacteria.
Used in Agricultural Industry:
In the agricultural industry, methyl stearidonate can be utilized as a natural antibacterial agent to protect crops from bacterial infections, thereby reducing the need for chemical pesticides and promoting sustainable farming practices.

Check Digit Verification of cas no

The CAS Registry Mumber 73097-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,9 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73097-00:
(7*7)+(6*3)+(5*0)+(4*9)+(3*7)+(2*0)+(1*0)=124
124 % 10 = 4
So 73097-00-4 is a valid CAS Registry Number.

73097-00-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (6E,9E,12E,15E)-octadeca-6,9,12,15-tetraenoate

1.2 Other means of identification

Product number -
Other names cis-6,9,12,15-Octadecatetraenoic acid methyl ester

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:73097-00-4 SDS

73097-00-4Relevant articles and documents

AN ALLELOPATHIC FATTY ACID FROM THE BROWN ALGA CLADOSIPHON OKAMURANUS

Kakisawa, Hiroshi,Asari, Fumika,Kusumi, Takenori,Toma, Takeshi,Sakurai, Takemaro,et al.

, p. 731 - 736 (1988)

An allelopathic substance was isolated from the methanol extract of the brown alga, Cladosiphon okamuranus.Extraction and purification of the active substance was monitored by bioassays against the conchospores of Porphyra yezoensis and Heterosigma akashiwo.The compound was identified as 6Z,9Z,12Z,15Z/octadecatetraenoic acid and its activity was then tested againts 36 species of microalgae.Many of eukaryotes tested were affected at 5 ppm, but prokaryotes were unaffected at 25 ppm.The tetraunsaturated fatty acid exterminated toxic red tide planktons such as Chattonella antiqua at 1 ppm concentration.Key Word Index-Cladosiphon okamuranus; Chordariaceae; brown alga; allelopathy; red tide; toxic phytoplankton; fatty acid; octadecatetraenoic acid.

Concise syntheses of three ω-3 polyunsaturated fatty acids

Jakobsen, Martin Gjerde,Vik, Anders,Hansen, Trond Vidar

, p. 5837 - 5839 (2013/01/13)

The synthesis of the three ω-3 polyunsaturated fatty acids, eicosatetraenoic acid (3), docosapentaenoic acid (4), and stearidonic acid (5) has been achieved using eicosapentaenoic acid or docosahexaenoic acid as the starting materials.

A new digalactosyl diacylglycerol from a cultured marine dinoflagellate Heterocapsa circularisquama

Hiraga, Yoshikazu,Kaku, Ken,Omoda, Daisuke,Sugihara, Kinuko,Hosoya, Hiroshi,Hino, Mizuki

, p. 1494 - 1496 (2007/10/03)

A new digalactosyl diacylglycerol (1) has been isolated from the cultured marine dinoflagellate Heterocapsa circularisquama together with known monogalactosyl diacylglycerols 2 and 3, and their structures were elucidated by spectroscopic methods. The digalactosyl diacylglycerol 1 showed cytolytic activity toward heart cells of oysters.

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