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13099-34-8

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13099-34-8 Usage

Description

17-Hydroxyheptadecanoic Acid is a hydroxylated fatty acid that is naturally occurring and has been identified in aeolian particles collected on the Frioul Islands and in the outer bark of E. globulus. This organic compound is characterized by the presence of a hydroxyl group attached to a long-chain fatty acid, which may contribute to its unique properties and potential applications.

Uses

Used in Chemical Research:
17-Hydroxyheptadecanoic Acid is used as a subject of study in chemical research for its unique structure and properties. Researchers are interested in understanding its chemical behavior, potential reactions, and how it can be synthesized or extracted for various applications.
Used in Environmental Science:
In environmental science, 17-Hydroxyheptadecanoic Acid is used as a biomarker for the presence of aeolian particles and as an indicator of environmental conditions on the Frioul Islands. Its detection in these particles can provide insights into atmospheric processes and the transport of organic compounds.
Used in Pharmaceutical Development:
17-Hydroxyheptadecanoic Acid is used as a potential pharmaceutical candidate due to its unique structure and presence in natural sources. Researchers are exploring its potential therapeutic properties, such as anti-inflammatory, antimicrobial, or other medicinal applications, which could lead to the development of new drugs.
Used in Cosmetics and Personal Care Products:
In the cosmetics and personal care industry, 17-Hydroxyheptadecanoic Acid may be used as an ingredient for its emollient, moisturizing, or conditioning properties. Its presence in natural sources like the outer bark of E. globulus suggests that it could be a sustainable and eco-friendly alternative to synthetic ingredients.
Used in Industrial Applications:
17-Hydroxyheptadecanoic Acid may also find use in various industrial applications, such as the production of lubricants, surfactants, or other specialty chemicals. Its unique properties could make it a valuable component in the development of new products or the improvement of existing ones.

Check Digit Verification of cas no

The CAS Registry Mumber 13099-34-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,9 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13099-34:
(7*1)+(6*3)+(5*0)+(4*9)+(3*9)+(2*3)+(1*4)=98
98 % 10 = 8
So 13099-34-8 is a valid CAS Registry Number.

13099-34-8SDS

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 17-HYDROXYHEPTADECANOIC ACID

1.2 Other means of identification

Product number -
Other names Heptadecanoic acid,17-hydroxy

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:13099-34-8 SDS

13099-34-8Relevant articles and documents

Process of preparing ω-hydroxy acids

-

, (2008/06/13)

A new synthesis of ω-hydroxy acids, which employs commercially available starting materials and lowers the cost of production. The process involves coupling a fatty acyl group by enamine chemistry, followed by a ring expansion and selective reduction of ketoacid.

Acides gras marques en position ω par un nucleide radioactif emetteur γ

Riche, Francoise,Mathieu, Jean-Paul,Vincens, Maurice,Bardy, Andre,Comet, Michel,Vidal, Michel

, p. 49 - 55 (2007/10/02)

The synthesis of many saturated, acetylenic, olefinic (Z or E) fatty acids labeled with 123I or 131I at the ω-position has been achieved.The radioactive iodine atom is introduced by a I-, *I- exchange reaction; the influence on the yield of several parameters - presence of iodine carrier, fatty acid and water concentrations, solution acidity - has been studied.Experimental conditions which produce labeling yields higher than 95percent have been defined; these results have lead to a very easy labeling method used in several hospitals in the external study of myocardial metabolism of fatty acids.

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