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Merck
CN

605573

棕榈酸-13C16

99 atom % 13C, 99% (CP)

别名:

十六烷酸-13C16

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关于此项目

线性分子式:
13CH3(13CH2)1413CO2H
化学文摘社编号:
分子量:
272.31
NACRES:
NA.12
PubChem Substance ID:
UNSPSC Code:
12352106
MDL number:
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产品名称

棕榈酸-13C16, 99 atom % 13C, 99% (CP)

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

SMILES string

[13CH3][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13C](O)=O

InChI key

IPCSVZSSVZVIGE-BZDICNBSSA-N

isotopic purity

99 atom % 13C

assay

99% (CP)

form

solid

mp

61-64 °C

mass shift

M+16

storage temp.

room temp

Quality Level

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Packaging

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存储类别

11 - Combustible Solids

wgk

nwg

flash_point_f

402.8 °F - closed cup

flash_point_c

206 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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
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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