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Safety Information

86033

Sigma-Aldrich

Sulfamide

purum, ≥99%

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10 G
¥5,680

¥5,680

Estimated to ship onJune 02, 2025

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10 G
¥5,680

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

¥5,680

Estimated to ship onJune 02, 2025

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

86033-BULK:
86033-50G:
86033-VAR:
86033-10G:

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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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