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492752

Sigma-Aldrich

Palmitic acid-2-13C

99 atom % 13C

Synonym(s):

Hexadecanoic acid-2-13C

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About This Item

Linear Formula:
CH3(CH2)1313CH2CO2H
CAS Number:
Molecular Weight:
257.42
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:

Note: This product can be packaged on demand. For information on pricing, availability and packaging of custom sizes, please contact Stable Isotopes Customer Service

isotopic purity

99 atom % 13C

Quality Level

mp

61-64 °C (lit.)

mass shift

M+1

SMILES string

CCCCCCCCCCCCCC[13CH2]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)/i15+1

InChI key

IPCSVZSSVZVIGE-XPOOIHDOSA-N

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This Item
Z370762Z131121Z720445
material

polypropylene

material

polypropylene

material

polypropylene

material

polymethylpentene

volume measuring range

2000 mL

volume measuring range

1000 mL

volume measuring range

1000 mL, accuracy: 5.0 mL

volume measuring range

2000 mL, accuracy: 12.0 mL

manufacturer/tradename

Bel-Art F28461-2000

manufacturer/tradename

Bel-Art F28461-1000

manufacturer/tradename

Nalgene 3662-1000

manufacturer/tradename

Nalgene 3663-2000

packaging

pack of 1 ea

packaging

pack of 1 ea

packaging

pack of 1 ea, case of 6 ea

packaging

pack of 1 ea, case of 4 ea

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

402.8 °F - closed cup

flash_point_c

206.00 °C - closed cup


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Mossakows, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry, 80 (2018)
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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 162(1) (2013)
Genotype--phenotype analysis of TCF4 mutations causing Pitt-Hopkins syndrome shows increased seizure activity with missense mutations
Rosenfeld, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 11(11), 797-797 (2009)

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