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605573

Sigma-Aldrich

棕榈酸-13C16

99 atom % 13C, 99% (CP)

别名:

十六烷酸-13C16

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About This Item

线性分子式:
13CH3(13CH2)1413CO2H
CAS号:
56599-85-0
分子量:
272.31
MDL编号:
MFCD00145066
UNSPSC代码:
12352106
PubChem化学物质编号:
24881914
NACRES:
NA.12

同位素纯度

99 atom % 13C

质量水平

200

方案

99% (CP)

表单

solid

mp

61-64 °C

质量偏移

M+16

储存温度

room temp

SMILES字符串

[13CH3][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13C](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)/i1+1,2+1,3+1,4+1,5+1,6+1,7+1,8+1,9+1,10+1,11+1,12+1,13+1,14+1,15+1,16+1

InChI key

IPCSVZSSVZVIGE-BZDICNBSSA-N

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储存分类代码

11 - Combustible Solids

WGK

nwg

闪点(°F)

402.8 °F - closed cup

闪点(°C)

206 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MBBC7786
MBBC4166
MBBC1633
MBBC1364
MBBB8879V

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Lei Chen et al.
Gastroenterology, 158(4), 985-999 (2019-11-25)
Functions of intestinal stem cells (ISCs) are regulated by diet and metabolic pathways. Hepatocyte nuclear factor 4 (HNF4) family are transcription factors that bind fatty acids. We investigated how HNF4 transcription factors regulate metabolism and their functions in ISCs in
Riccardo M Betto et al.
Nature genetics, 53(2), 215-229 (2021-02-03)
Naive epiblast and embryonic stem cells (ESCs) give rise to all cells of adults. Such developmental plasticity is associated with genome hypomethylation. Here, we show that LIF-Stat3 signaling induces genomic hypomethylation via metabolic reconfiguration. Stat3-/- ESCs show decreased α-ketoglutarate production
Matteo Audano et al.
The Journal of cell biology, 220(3) (2021-02-11)
The commitment of mesenchymal stem cells to preadipocytes is stimulated by hormonal induction. Preadipocytes induced to differentiate repress protein synthesis, remodel their cytoskeleton, and increase mitochondrial function to support anabolic pathways. These changes enable differentiation into mature adipocytes. Our understanding
M Zaeem Cader et al.
Cell, 180(2), 278-295 (2020-01-25)
Mutations in FAMIN cause arthritis and inflammatory bowel disease in early childhood, and a common genetic variant increases the risk for Crohn's disease and leprosy. We developed an unbiased liquid chromatography-mass spectrometry screen for enzymatic activity of this orphan protein.

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