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119176-67-9

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119176-67-9 Usage

Uses

Nonanedioic-D14 acid is a labelled analogue of Nonanedioic acid, a bioactive molecule used in treating acne and other skin disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 119176-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,1,7 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 119176-67:
(8*1)+(7*1)+(6*9)+(5*1)+(4*7)+(3*6)+(2*6)+(1*7)=139
139 % 10 = 9
So 119176-67-9 is a valid CAS Registry Number.

119176-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,9-NONANEDIOIC-D14 ACID

1.2 Other means of identification

Product number -
Other names Nonanedioic-D14 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:119176-67-9 SDS

119176-67-9Upstream product

119176-67-9Relevant articles and documents

Synthesis of deuterated [D32]oleic acid and its phospholipid derivative [D64]dioleoylsn- glycero-3-phosphocholine

Darwish, Tamim A.,Luks, Emily,Moraes, Greta,Yepuri, Nageshwar R.,Holden, Peter J.,Jamesa, Michael

, p. 520 - 529 (2014/03/21)

Oleic acid and its phospholipid derivatives are fundamental to the structure and function of cellular membranes. As a result, there has been increasing interest in the availability of their deuterated forms for many nuclear magnetic resonance, infrared, mass spectroscopy and neutron scattering studies. Here, we present for the first time a straightforward, large-scale (gram quantities) synthesis of highly deuterated [D32]oleic acid by using multiple, yet simple and high yielding reactions. The precursors for the synthesis of [D32]oleic acid are [D14]azelaic acid and [D17]nonanoic acid, which were obtained by complete deuteration (>98% D) of their 1H forms by using metal catalysed hydrothermal H/D exchange reactions. The oleic acid was producedwith ca. 94% D isotopic purity and with no contamination by the trans-isomer (elaidic acid). The subsequent synthesis of [D64]dioleoyl-sn-glycero-3-phosphocholine from [D32]oleic acid is also described. Copyright

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