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Merck
CN

86329

Sigma-Aldrich

牛磺酸

≥99.5% (T), suitable for UHPLC, BioUltra

别名:

2-氨基乙磺酸

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About This Item

线性分子式:
NH2CH2CH2SO3H
CAS号:
分子量:
125.15
Beilstein:
1751215
EC 号:
MDL编号:
UNSPSC代码:
12352106
PubChem化学物质编号:
NACRES:
NA.26

产品名称

牛磺酸, BioUltra, ≥99.5% (T)

产品线

BioUltra

质量水平

方案

≥99.5% (T)

表单

powder or crystals

技术

UHPLC: suitable

杂质

insoluble matter, passes filter test

灼烧残渣 (900 °C)

≤0.05%

颜色

colorless to white

pH值(酸碱度)

4.5-6.0 (25 °C, 0.5 M in H2O)

mp

>300 °C (lit.)

溶解性

H2O: 0.5 M at 20 °C, clear, colorless

痕量阴离子

chloride (Cl-): ≤50 mg/kg
sulfate (SO42-): ≤500 mg/kg

痕量阳离子

Al: ≤5 mg/kg
As: ≤0.1 mg/kg
Ba: ≤5 mg/kg
Bi: ≤5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Li: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
Na: ≤200 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg

λ

0.5 M in H2O

紫外吸收

λ: 260 nm Amax: 0.006
λ: 280 nm Amax: 0.005

应用

cell analysis

SMILES字符串

NCCS(O)(=O)=O

InChI

1S/C2H7NO3S/c3-1-2-7(4,5)6/h1-3H2,(H,4,5,6)

InChI key

XOAAWQZATWQOTB-UHFFFAOYSA-N

基因信息

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生化/生理作用

甘氨酸受体的非选择性内源激动剂。
甘氨酸受体的非选择性内源激动剂。在某些细胞中调节细胞凋亡的条件必需磺化氨基酸;在许多新陈代谢活动中起作用;是蛋氨酸和半胱氨酸的代谢产物。

其他说明

牛磺酸的生物作用;NCTC培养基的组成成分

储存分类代码

13 - Non Combustible Solids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

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

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访问文档库

Taurine: biological update.
C E Wright et al.
Annual review of biochemistry, 55, 427-453 (1986-01-01)
CHEMICALLY DEFINED MEDIA FOR CULTIVATION OF LONG-TERM CELL STRAINS FROM FOUR MAMMALIAN SPECIES.
V J EVANS et al.
Experimental cell research, 36, 439-474 (1964-12-01)
M Axelson et al.
Hepatology (Baltimore, Md.), 31(6), 1305-1312 (2000-05-29)
The biosynthesis of bile acids by primary cultures of normal human hepatocytes has been investigated. A general and sensitive method for the isolation and analysis of sterols and bile acids was used, based on anion exchange chromatography and gas chromatography-mass
Tsutomu Suzuki et al.
Wiley interdisciplinary reviews. RNA, 2(3), 376-386 (2011-10-01)
Mitochondrial DNA mutations that cause mitochondrial dysfunction are responsible for a wide spectrum of human diseases, referred to as mitochondrial diseases. Pathogenic point mutations are found frequently in genes encoding mitochondrial (mt) tRNAs, indicating that impaired functioning of mutant mt
Marlene Wewalka et al.
The Journal of clinical endocrinology and metabolism, 99(4), 1442-1451 (2014-01-18)
Bile acids (BAs) are newly recognized signaling molecules in glucose and energy homeostasis. Differences in BA profiles with type 2 diabetes mellitus (T2D) remain incompletely understood. The objective of the study was to assess serum BA composition in impaired glucose-tolerant

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