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366897

Sigma-Aldrich

Palmitic acid-d31

98 atom % D, 99% (CP)

Synonym(s):

Hexadecanoic-d31 acid

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About This Item

Linear Formula:
CD3(CD2)14CO2H
CAS Number:
39756-30-4
Molecular Weight:
287.62
MDL number:
MFCD00053335
UNSPSC Code:
12352106
PubChem Substance ID:
24862721
NACRES:
NA.12

isotopic purity

98 atom % D

assay

99% (CP)

form

solid

mp

61-64 °C

mass shift

M+31

SMILES string

[2H]C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C(O)=O

InChI

1S/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)/i1D3,2D2,3D2,4D2,5D2,6D2,7D2,8D2,9D2,10D2,11D2,12D2,13D2,14D2,15D2

InChI key

IPCSVZSSVZVIGE-SAQPIRCFSA-N

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General description

Palmitic acid-d31 is an isotopic analogue of palmitic acid.

Application

Palmitic acid-d31 can be used in the synthesis of saturated and unsaturated fatty acids. It is used in quantitative determination of fatty acids from plastic labware.

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Storage Class

11 - Combustible Solids

wgk_germany

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Fu-Lin E Chu et al.
Molecular and biochemical parasitology, 119(2), 179-190 (2002-01-30)
The capability of synthesizing fatty acids de novo in the meront stage of the oyster protozoan parasite, Perkinsus marinus, was investigated employing stable-isotope-labeled precursors (1,2 13C-acetate and palmitic-d(31) acid). Fatty acid methyl esters derived from 1,2 13C-acetate and palmitic-d(31) acid
Wolf, R.R.
Radioactive and Stable Isotope Tracers in Biomedicine: Principles and Practice of Kinetic Analysis, 322-322 (1992)
Avarzed Amgalanbaatar et al.
Lipids, 50(8), 799-804 (2015-07-01)
This study demonstrated that the cells of Helicobacter felis and Helicobacter cinaedi spontaneously absorb cholesterol added to the medium. A recent study by our group has revealed that phosphatidylethanolamine (PtdEtn) of Helicobacter pylori contains myristic acid as the most predominant

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