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Merck
CN

86040

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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线性分子式:
NH2SO3H
化学文摘社编号:
5329-14-6
分子量:
97.09
NACRES:
NA.25
PubChem Substance ID:
329769435
UNSPSC Code:
12161700
EC Number:
226-218-8
MDL number:
MFCD00011603

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产品名称

氨基磺酸, analytical standard (for acidimetry), ACS reagent

InChI key

IIACRCGMVDHOTQ-UHFFFAOYSA-N

InChI

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

SMILES string

NS(O)(=O)=O

grade

ACS reagent
analytical standard (for acidimetry)

agency

complies with DIN 19266

assay

99.3-100.3% (dried material)

mp

215-225 °C (dec.) (lit.)

anion traces

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

cation traces

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

application(s)

environmental
food and beverages
general analytical
industrial qc
pharmaceutical

format

mixture

Quality Level

100

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Application

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。

Features and Benefits

  • 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)

General description

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。

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCP0139
BCCM5328
BCCL2006
BCCM3324
BCCK1487

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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
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
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
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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