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29907-56-0

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29907-56-0 Usage

Description

9,12,13-trihydroxy-10-octadecenoic acid, also known as a TriHOME (Trihydroxy fatty acid ester of hydroxyoctadecenoic acid), is a unique fatty acid derivative characterized by the presence of three hydroxy substituents at positions 9, 12, and 13 along the octadec-10-enoic acid chain. 9,12,13-trihydroxy-10-octadecenoic acid exhibits distinct chemical properties due to its hydroxyl groups, which can potentially interact with various biomolecules and macromolecules.

Uses

Used in Pharmaceutical Applications:
9,12,13-trihydroxy-10-octadecenoic acid is used as a pharmaceutical compound for its potential therapeutic effects. The hydroxyl groups present in the molecule allow for interactions with biopolymers and macromolecules, making it a promising candidate for the development of new drugs and therapies.
Used in Drug Delivery Systems:
In the field of drug delivery, 9,12,13-trihydroxy-10-octadecenoic acid can be utilized as a component in the design of novel drug delivery systems. Its unique structure and functional groups can be exploited to enhance the delivery, bioavailability, and therapeutic outcomes of various drugs, particularly those targeting specific biological pathways or molecular targets.
Used in Cosmetics Industry:
9,12,13-trihydroxy-10-octadecenoic acid is used as an active ingredient in the cosmetics industry for its potential benefits to skin health. 9,12,13-trihydroxy-10-octadecenoic acid's ability to interact with skin biomolecules may contribute to improved skin hydration, elasticity, and overall skin quality.
Used in Research and Development:
In the research and development sector, 9,12,13-trihydroxy-10-octadecenoic acid serves as a valuable compound for studying the effects of hydroxyl group substitutions on the properties and interactions of fatty acid derivatives. This knowledge can be applied to the development of new materials, drugs, and other applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 29907-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,0 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29907-56:
(7*2)+(6*9)+(5*9)+(4*0)+(3*7)+(2*5)+(1*6)=150
150 % 10 = 0
So 29907-56-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H34O5/c1-2-3-7-11-16(20)17(21)14-13-15(19)10-8-5-4-6-9-12-18(22)23/h13-17,19-21H,2-12H2,1H3,(H,22,23)/b14-13+

29907-56-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 9,12,13-trihydroxy-10-octadecaenoic acid

1.2 Other means of identification

Product number -
Other names 10-Octadecenoic acid,9,12,13-trihydroxy-

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:29907-56-0 SDS

29907-56-0Downstream Products

29907-56-0Relevant articles and documents

Structural Elucidation of Naturally Occurring 9,12,13-Trihydroxy Fatty Acids by a Synthetic Study

Kato, Tadahiro,Yamaguchi, Yoshihiro,Hirukawa, Toshifumi,Hoshino, Naoko

, p. 1349 - 1357 (2007/10/02)

Our investigation on anti-rice blast fungus materials from the rice plant has already led to the isolation of various types of oxygenated unsaturated fatty acids, which play an essential role in the defense of the rice plant against this fungus.Among those isolated were 9,12,13-trihydroxy C-18 fatty acids.We have determined the relative stereochemistry of the trihydroxy acid by synthesizing the possible stereoisomers.This paper describes the details of our synthetic study, demonstrating the fatty acid to be 9S,12S,13S-trihydroxyoctadeca-10E,15Z-dienoic acid and its 15-dihydro analogue.The absolute configuration was determined by observing a positive Cotton effect in the CD spectrum of the benzoate derivative of the natural material.

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