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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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关于此项目

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
此项目有

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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Christopher S Adams et al.
Journal of the American Chemical Society, 134(26), 10807-10810 (2012-06-20)
Nitrogen-containing stereotriads, compounds with three adjacent stereodefined carbons, are commonly found in biologically important molecules. However, the preparation of molecules bearing these motifs can be challenging. Herein, we describe a modular oxidation protocol which converts a substituted allene to a
Cobalt-catalyzed direct arylation and benzylation by C-H/C-O cleavage with sulfamates, carbamates, and phosphates.
Weifeng Song et al.
Angewandte Chemie (International ed. in English), 51(33), 8251-8254 (2012-07-14)
Derek J Langeslay et al.
Glycobiology, 22(9), 1173-1182 (2012-05-18)
Sulfamate groups (NHSO(3)(-)) are important structural elements in the glycosaminoglycans (GAGs) heparin and heparan sulfate (HS). In this work, proton nuclear magnetic resonance (NMR) line-shape analysis is used to explore the solvent exchange properties of the sulfamate NH groups within
Keisuke Takahashi et al.
Organic letters, 14(6), 1644-1647 (2012-03-07)
A total synthesis of (-)-kaitocephalin, an ionotropic glutamate receptor antagonist, is accomplished in highly stereocontrolled manner via Overman rearrangement, rhodium-catalyzed benzylic C-H amination, pyrrolidine formation involving nucleophilic opening of a cyclic sulfamate, and rhodium-catalyzed allylic C-H amination as key steps.
Liana Hie et al.
Organic letters, 14(16), 4182-4185 (2012-08-02)
A facile nickel-catalyzed method to achieve the amination of synthetically useful aryl sulfamates and carbamates is reported. Contrary to most Ni-catalyzed amination reactions, this user-friendly approach relies on an air-stable Ni(II) precatalyst, which, when employed with a mild reducing agent
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