01-5060
Ammonium sulfamate
JIS special grade, ≥98.5%
Iniciar sesión para ver los precios por organización y contrato.
Seleccione un Tamaño
Cambiar Vistas
Acerca de este artículo
Fórmula lineal:
NH4SO3NH2
Número CAS:
Peso molecular:
114.12
UNSPSC Code:
12352301
PubChem Substance ID:
EC Number:
231-871-7
MDL number:
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarlegrade
JIS special grade
assay
≥98.5%
form
crystalline
availability
available only in Japan
pH
4.5-6.0 (25 °C, 114.1 g/L)
mp
131-135 °C (lit.)
SMILES string
N.NS(O)(=O)=O
InChI
1S/H3NO3S.H3N/c1-5(2,3)4;/h(H3,1,2,3,4);1H3
InChI key
GEHMBYLTCISYNY-UHFFFAOYSA-N
Clase de almacenamiento
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Elija entre una de las versiones más recientes:
¿Ya tiene este producto?
Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
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
Derek J Langeslay et al.
Analytical chemistry, 83(20), 8006-8010 (2011-09-15)
Sulfamate (NHSO(3)(-)) groups are critically important structural elements of the glycosaminoglycans heparin and heparan sulfate (HS). Experimental conditions are presented for detection of the sulfamate (1)H NMR resonances in aqueous solution. NMR spectra reported for N-sulfoglucosamine (GlcNS) and the synthetic
Toolika Agrawal et al.
Organic letters, 15(1), 96-99 (2012-12-19)
The iron-catalyzed cross-coupling of aryl sulfamates and tosylates has been achieved with primary and secondary alkyl Grignards. This study of iron-catalyzed cross-coupling reactions also examines the isomerization and β-hydride elimination problems that are associated with the use of isopropyl nucleophiles.