跳转至内容
Merck
CN

605573

Sigma-Aldrich

棕榈酸-13C16

99 atom % 13C, 99% (CP)

别名:

十六烷酸-13C16

登录查看公司和协议定价


About This Item

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

同位素纯度

99 atom % 13C

质量水平

检测方案

99% (CP)

形式

solid

mp

61-64 °C

质量偏移

M+16

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

正在寻找类似产品? 访问 产品对比指南

包装

这种产品可以散装供应,并可按需包装。有关定价、供货和包装的信息,请联系稳定同位素客户服务

WGK

nwg

闪点(°F)

closed cup

闪点(°C)

closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

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.

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门