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2-Octadecenoic acid, also known as oleic acid, is a monounsaturated fatty acid with the chemical formula C18H34O2. It is a common component of various vegetable oils, such as olive oil, and is known for its health benefits, including reducing inflammation and improving heart health. This 18-carbon fatty acid has a double bond at the ninth carbon atom, which gives it its characteristic properties. Oleic acid plays a crucial role in the human diet and is also used in the production of soaps, cosmetics, and biodiesel.

5340-63-6

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5340-63-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5340-63-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5340-63:
(6*5)+(5*3)+(4*4)+(3*0)+(2*6)+(1*3)=76
76 % 10 = 6
So 5340-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h16-17H,2-15H2,1H3,(H,19,20)/b17-16-

5340-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name OCTADECAN-2-OIC ACID, 2-HYDROXY

1.2 Other means of identification

Product number -
Other names octadecenic 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:5340-63-6 SDS

5340-63-6Upstream product

5340-63-6Relevant academic research and scientific papers

Synthesis of Long Chain Substituted cis- and trans-2-Trichloromethyldioxolanones.

Mukarram, Mohammad,Ahmad, Ishtiaque,Ahmad, Mashood

, p. 1949 - 1962 (2007/10/02)

Reaction of chloral hydrate with α-hydroxy derivatives of palmitic (Ia), stearic (Ib) and behenic (Ic) acids gave the corresponding cis-2-trichloromethyldioxolanones (IIa,b,c) and trans-2-trichloromethyldioxolanones (IIIa,b,c), yields being ca. 50percent for each reaction product.The structures of the individual reaction products were established clearly by elemental analysis as well as by spectral studies.

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