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10030-73-6

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10030-73-6 Usage

Uses

Palmitelaidic Acid is the 9E-isomer of Palmitoleic Acid (P144900); a polyunsaturated fatty acid which contributes to reduced protein oxidation in mammals.

Definition

ChEBI: A straight-chain, monounsaturated, 16-carbon fatty acid with a trans-double bond at position C-9; the trans-isomer of palmitoleic acid and predominant trans-16:1 isomer in cheeses from goat and ewe milk. Major dietary sources are artly hydrogenated vegetable oils.

Check Digit Verification of cas no

The CAS Registry Mumber 10030-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,3 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10030-73:
(7*1)+(6*0)+(5*0)+(4*3)+(3*0)+(2*7)+(1*3)=36
36 % 10 = 6
So 10030-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h7-8H,2-6,9-15H2,1H3,(H,17,18)/b8-7+

10030-73-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name palmitelaidic acid

1.2 Other means of identification

Product number -
Other names TRANS-9-HEXADECENOIC 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:10030-73-6 SDS

10030-73-6Relevant articles and documents

-

Ames et al.

, p. 268 (1968)

-

Phosphonium Iodide in Organic Synthesis

Chatterjea, J. N.,Majee, R. N.,Mukherjee, S. N.

, p. 733 - 735 (2007/10/02)

Phosphonium iodide is found useful in the stereospecific conversion of some vicinal diols to olefins.Synthesis of cis-hexadec-9-enolide has been achieved.

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