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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:
107-35-7
分子量:
125.15
NACRES:
NA.26
PubChem Substance ID:
57653091
UNSPSC Code:
12352106
EC Number:
203-483-8
MDL number:
MFCD00008197
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

200

Gene Information

rat ... Ppm1a(24666)

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相关类别

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
BCCN8873
BCCL2691
BCCM4680
BCCK7199
BCCJ6551

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V J EVANS et al.
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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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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
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