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Merck
CN

86329

牛磺酸

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

别名:

2-氨基乙磺酸

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关于此项目

线性分子式:
NH2CH2CH2SO3H
化学文摘社编号:
分子量:
125.15
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
203-483-8
MDL number:
Beilstein/REAXYS Number:
1751215
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产品名称

牛磺酸, BioUltra, ≥99.5% (T)

InChI

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

SMILES string

NCCS(O)(=O)=O

InChI key

XOAAWQZATWQOTB-UHFFFAOYSA-N

product line

BioUltra

assay

≥99.5% (T)

form

powder or crystals

technique(s)

UHPLC: suitable

impurities

insoluble matter, passes filter test

ign. residue (900 °C)

≤0.05%

color

colorless to white

pH

4.5-6.0 (25 °C, 0.5 M in H2O)

mp

>300 °C (lit.)

solubility

H2O: 0.5 M at 20 °C, clear, colorless

anion traces

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

cation traces

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

UV absorption

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

application(s)

cell analysis

Quality Level

Gene Information

rat ... Ppm1a(24666)

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Biochem/physiol Actions

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。

Other Notes

牛磺酸的生物作用;NCTC培养基的组成成分

存储类别

13 - Non Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

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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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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