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86033

Sigma-Aldrich

Sulfamide

purum, ≥99%

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10 G
504,00 kr

504,00 kr

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10 G
504,00 kr

About This Item

Linear Formula:
(NH2)2SO2
CAS Number:
7803-58-9
Molecular Weight:
96.11
EC Number:
232-262-9
MDL number:
MFCD00011606
UNSPSC Code:
12352100
PubChem Substance ID:
329769434
NACRES:
NA.22

504,00 kr

Please contact Customer Service for Availability
Request a Bulk Order

grade

purum

Quality Level

100

Assay

≥99%

form

powder

mp

90-92 °C (lit.)
90-92 °C

density

1.611 g/mL at 25 °C (lit.)

SMILES string

NS(N)(=O)=O

InChI

1S/H4N2O2S/c1-5(2,3)4/h(H4,1,2,3,4)

InChI key

NVBFHJWHLNUMCV-UHFFFAOYSA-N

Gene Information

human ... CA1(759) , CA2(760)

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD5505

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The role of sulfamide derivatives in medicinal chemistry: a patent review
Reitz AB, et al.
Expert Opinion on Therapeutic Patents, 19(10), 1449-1453 (2009)
Sulfamides and sulfamide polymers directly from sulfur dioxide.
Leontiev AV, et al.
Chemical Communications (Cambridge, England), 2887-2889 (2006)
Laura Rosanò et al.
Cancer research, 74(24), 7453-7464 (2014-11-08)
The high mortality of epithelial ovarian cancer (EOC) is mainly caused by resistance to the available therapies. In EOC, the endothelin-1 (ET-1, EDN1)-endothelin A receptor (ETAR, EDNRA) signaling axis regulates the epithelial-mesenchymal transition (EMT) and a chemoresistant phenotype. However, there
Stephen T Vito et al.
Toxicology and applied pharmacology, 281(2), 185-194 (2014-12-03)
Tetramethylenedisulfotetramine (TETS) is a potent convulsant poison for which there is currently no approved antidote. The convulsant action of TETS is thought to be mediated by inhibition of type A gamma-aminobutyric acid receptor (GABAAR) function. We, therefore, investigated the effects

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