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19629-78-8

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19629-78-8 Usage

Structure

A 16-carbon saturated fatty acid chain with a phenyl group attached to the hexadecanoic acid molecule

Industries

Used in pharmaceuticals, cosmetics, and as a component in organic synthesis

Potential properties

Anti-inflammatory, antimicrobial, and ability to modulate lipid metabolism

Drug delivery agent

Capable of forming stable micelles and liposomes

Ongoing research

Various potential applications and further study into its properties and uses

Check Digit Verification of cas no

The CAS Registry Mumber 19629-78-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,2 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19629-78:
(7*1)+(6*9)+(5*6)+(4*2)+(3*9)+(2*7)+(1*8)=148
148 % 10 = 8
So 19629-78-8 is a valid CAS Registry Number.
InChI:InChI=1/C22H36O2/c23-22(24)20-16-11-9-7-5-3-1-2-4-6-8-10-13-17-21-18-14-12-15-19-21/h12,14-15,18-19H,1-11,13,16-17,20H2,(H,23,24)

19629-78-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 16-PHENYLHEXADECANOIC ACID

1.2 Other means of identification

Product number -
Other names 16-phenyl-hexadecanoic 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:19629-78-8 SDS

19629-78-8Relevant articles and documents

SYNTHESIS OF 16-(4-IODOPHENYL)HEXADECANOIC ACID

Protiva, Jiri,Pecka, Jaroslav,Klinotova, Eva,Prochazka, Milos

, p. 872 - 878 (2007/10/02)

16-(4-Iodophenyl)hexadecanoic acid was prepared in six steps by two methods: from 6-(2-thienyl)hexanoic acid and 6-phenylhexanoyl chloride or by alkylation, or acylation, of 2-thienylthiophene.Mass and 1H NMR spectra of some prepared compounds are discussed.The synthesis is suitable for preparation of radioactively labelled acids used as myocardial imaging agents.

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