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Merck

28-5700

Sulfamic acid

JIS special grade, ≥99.5%

Synonym(s):

Amidosulfonic acid

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About This Item

Linear Formula:
NH2SO3H
CAS Number:
Molecular Weight:
97.09
UNSPSC Code:
12352106
PubChem Substance ID:
EC Number:
226-218-8
MDL number:
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Product Name

Sulfamic acid, JIS special grade, ≥99.5%

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

JIS special grade

assay

≥99.5%

form

solid

availability

available only in Japan

mp

215-225 °C (dec.) (lit.)

solubility

water: 213 g/L at 20 °C
water: 470 g/L at 80 °C

density

2.151 g/cm3 at 25 °C

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signalword

Warning

Hazard Classifications

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

Storage Class

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


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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)
Laszlo Tarko et al.
Bioorganic & medicinal chemistry, 21(6), 1404-1409 (2012-12-05)
The last version of the PRECLAV algorithm was used to investigate a series of sulfamate/sulfamide carbonic anhydrase (CA, EC 4.2.1.1) inhibitors. PRECLAV allows identification of outliers for lead hopping, significant molecular fragments and similarity computation of a calibration set vs.
Edward J Emmett et al.
Organic & biomolecular chemistry, 10(20), 4007-4014 (2012-03-13)
By using DABCO·(SO(2))(2), DABSO, as a solid bench-stable SO(2)-equivalent, the palladium-catalysed aminosulfonylation of aryl-, alkenyl- and heteroaryl halides has been achieved. N,N-Dialkylhydrazines are employed as the N-nucleophiles and provide N-aminosulfonamides as the products in good to excellent yields. The reactions
Ning Dai et al.
Environmental science & technology, 46(17), 9793-9801 (2012-07-27)
With years of full-scale experience for precombustion CO(2) capture, amine-based technologies are emerging as the prime contender for postcombustion CO(2) capture. However, concerns for postcombustion applications have focused on the possible contamination of air or drinking water supplies downwind by

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