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Merck
CN

86040

Supelco

氨基磺酸

analytical standard (for acidimetry), ACS reagent

别名:

氨基硫酸, 氨基磺酸, 磺酰胺酸

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About This Item

线性分子式:
NH2SO3H
CAS号:
分子量:
97.09
EC 号:
MDL编号:
UNSPSC代码:
12161700
PubChem化学物质编号:
NACRES:
NA.25

等级

ACS reagent
analytical standard (for acidimetry)

质量水平

Agency

complies with DIN 19266

方案

99.3-100.3% (dried material)

mp

215-225 °C (dec.) (lit.)

痕量阴离子

chloride (Cl-): ≤10 mg/kg
sulfate (SO42-): ≤500 mg/kg

痕量阳离子

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
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤10 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

应用

environmental
food and beverages
general analytical
industrial qc
pharmaceutical

包装形式

mixture

SMILES字符串

NS(O)(=O)=O

InChI

1S/H3NO3S/c1-5(2,3)4/h(H3,1,2,3,4)

InChI key

IIACRCGMVDHOTQ-UHFFFAOYSA-N

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一般描述

氨基磺酸是一种强无机酸,以晶体形式存在。干燥状态下性状稳定、不吸湿且无色无臭,便于商业包装和搬运。

应用

可用作分析应用的标酸基准物。
氨基磺酸还可在无水可视滴定、电导滴定和电位滴定中作为基准物使用。

特点和优势

  • 以坚固玻璃瓶装提供,确保开封前整个保质期内的稳定性。
  • 高质量提供准确的滴定度测定
  • 附详细的分析证书(CoA)

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

危险化学品

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

Amit Saha et al.
Chemical communications (Cambridge, England), 48(71), 8889-8891 (2012-07-21)
Unnatural α-amino acids containing dithiocarbamate side chains were synthesized by a one-pot reaction of in situ generated dithiocarbamate anions with sulfamidates. A wide range of these anions participated in the highly regio- and stereo-selective ring opening of sulfamidates to produce
Patricia Chávez et al.
The Journal of organic chemistry, 77(4), 1922-1930 (2012-01-31)
An intramolecular diamination of acrylates is reported using sulfamates as nitrogen sources. This reaction proceeds under palladium(II) catalysis with copper bromide as oxidant and gives rise to anti-configured 2,3-diamino carboxylates as bicyclic sulfamate derivatives. An aminobrominated intermediate within the diamination
Na Zhang et al.
The Journal of organic chemistry, 77(14), 5956-5964 (2012-06-21)
The efficiency of arylboron-based nucleophiles, boronic acid, potassium trifluoroborate, neopentylglycolboronate, and pinacol boronate in nickel-catalyzed Suzuki-Miyaura cross-coupling reactions with the two C-O electrophiles, mesylates, and sulfamates was compared. Arylboronic acid is the most reactive and most atom-economic of the four
Jean-Yves Winum et al.
Bioorganic & medicinal chemistry, 21(6), 1419-1426 (2012-12-04)
Targeting tumour associated carbonic anhydrase (CA, EC 4.2.1.1) isoforms IX and XII is now considered as a pertinent approach for the development of new cancer therapeutics against hypoxic tumours. In the last period, with the help of X-ray crystallography, much
Daniel Can et al.
Angewandte Chemie (International ed. in English), 51(14), 3354-3357 (2012-02-22)
Enhanced receptor selectivity: carbonic anhydrase inhibitors are relevant for both cancer diagnosis and therapy. Combining non-radioactive Re compounds with their radioactive (99m)Tc homologs enables the use of identical molecules for therapy and imaging (theragnostic). The syntheses and in vitro evaluation

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