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605700

Sigma-Aldrich

Palmitic acid-5,6,7,8-13C4

99 atom % 13C, 99% (CP)

Synonym(s):

Hexadecanoic-5,6,7,8-13C4 acid

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About This Item

Linear Formula:
CH3(CH2)7(13CH2)4(CH2)3CO2H
Molecular Weight:
260.39
MDL number:
MFCD01075555
UNSPSC Code:
12352202
PubChem Substance ID:
329759074
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

200

assay

99% (CP)

form

solid

mp

61-64 °C (lit.)

mass shift

M+4

SMILES string

CCCCCCCC[13CH2][13CH2][13CH2][13CH2]CCCC(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)/i9+1,10+1,11+1,12+1

InChI key

IPCSVZSSVZVIGE-BMHINFNASA-N

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This Item
Z112178Z112135Z112151
32mm Round cell window KBr, Undrilled

Z112119

32mm Round cell window

32mm Round cell window KBr, Drilled

Z112178

32mm Round cell window

32mm Round cell window BaF2, Undrilled

Z112135

32mm Round cell window

32mm Round cell window NaCl, Drilled

Z112151

32mm Round cell window

material

KBr

material

KBr

material

BaF2

material

NaCl

packaging

pkg of (contains 1 window)

packaging

pkg of (contains 1 window)

packaging

pkg of (contains 1 window)

packaging

pkg of (contains 1 window)

technique(s)

IR spectroscopy: suitable

technique(s)

IR spectroscopy: suitable

technique(s)

IR spectroscopy: suitable

technique(s)

IR spectroscopy: suitable

diam. × thickness

32 mm × 3 mm

diam. × thickness

32 mm × 3 mm

diam. × thickness

32 mm × 3 mm

diam. × thickness

32 mm × 3 mm

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

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Soonsang Yoon et al.
Journal of neuromuscular diseases, 5(1), 59-73 (2017-12-28)
Mutations in the LAMA2 gene encoding laminin-α2 cause congenital muscular dystrophy Type 1A (MDC1A), a severe recessive disease with no effective treatment. Previous studies have shown that aberrant activation of caspases and cell death through a pathway regulated by BAX
Jessica X Chong et al.
American journal of human genetics, 96(5), 841-849 (2015-05-11)
Multiple pterygium syndrome (MPS) is a phenotypically and genetically heterogeneous group of rare Mendelian conditions characterized by multiple pterygia, scoliosis, and congenital contractures of the limbs. MPS typically segregates as an autosomal-recessive disorder, but rare instances of autosomal-dominant transmission have
Catrin Sian Rutland et al.
Development (Cambridge, England), 138(18), 3955-3966 (2011-08-25)
The expression and function of embryonic myosin heavy chain (eMYH) has not been investigated within the early developing heart. This is despite the knowledge that other structural proteins, such as alpha and beta myosin heavy chains and cardiac alpha actin
Reha M Toydemir et al.
Nature genetics, 38(5), 561-565 (2006-04-28)
The genetic basis of most conditions characterized by congenital contractures is largely unknown. Here we show that mutations in the embryonic myosin heavy chain (MYH3) gene cause Freeman-Sheldon syndrome (FSS), one of the most severe multiple congenital contracture (that is
Sachiko Homma et al.
Skeletal muscle, 6(1), 42-42 (2016-12-03)
Nuclear bodies, such as nucleoli, PML bodies, and SC35 speckles, are dynamic sub-nuclear structures that regulate multiple genetic and epigenetic processes. Additional regulation is provided by RNA/DNA handling proteins, notably TDP-43 and FUS, which have been linked to ALS pathology.

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