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Sulfamide

CAS No.
7803-58-9
Chemical Name:
Sulfamide
Synonyms
SULFURIC DIAMIDE;SULPHAMIDE;SulfaMid;famide;NSC 252;SULFAMIDE;Suleamide;[S(NH2)2O2];Sulfamamide;Sulfamide >
CBNumber:
CB2488651
Molecular Formula:
H4N2O2S
Molecular Weight:
96.11
MDL Number:
MFCD00011606
MOL File:
7803-58-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 00:35:10
Product description Number Pack Size Price
Sulfamide 99% 211370 5g $39.7
Sulfamide 99% 211370 25g $94.1
Sulfamide >96.0%(N) S0890 25g $29
Sulfamide >96.0%(N) S0890 250g $134
Sulfamide Asreported 289072 100g $333
More product size

Sulfamide Properties

Melting point 90-92 °C(lit.)
Density 1.611 g/mL at 25 °C(lit.)
storage temp. Inert atmosphere,Room Temperature
solubility water: soluble50mg/mL, clear, colorless to faintly yellow
form Crystalline Powder, Free From Visible Impurities
pka 10.87±0.60(Predicted)
color White to practically white , free from visible impurities
PH 5.67 at 21.7℃ and 10g/L
Water Solubility soluble
Sensitive Moisture Sensitive
Merck 14,8922
InChI 1S/H4N2O2S/c1-5(2,3)4/h(H4,1,2,3,4)
InChIKey NVBFHJWHLNUMCV-UHFFFAOYSA-N
SMILES NS(N)(=O)=O
CAS DataBase Reference 7803-58-9(CAS DataBase Reference)
FDA UNII VS7TZW634V
NIST Chemistry Reference Sulfamide(7803-58-9)
EPA Substance Registry System Sulfamide (7803-58-9)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  3
9
TSCA  TSCA listed
HazardClass  IRRITANT
HS Code  28530090
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
REACH Registrations Active
NFPA 704
0
1 0

Sulfamide price More Price(81)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 211370 Sulfamide 99% 7803-58-9 5g $39.7 2026-04-30 Buy
Sigma-Aldrich 211370 Sulfamide 99% 7803-58-9 25g $94.1 2026-04-30 Buy
TCI Chemical S0890 Sulfamide >96.0%(N) 7803-58-9 25g $29 2026-04-30 Buy
TCI Chemical S0890 Sulfamide >96.0%(N) 7803-58-9 250g $134 2026-04-30 Buy
Usbiological 289072 Sulfamide Asreported 7803-58-9 100g $333 2026-06-03 Buy
Product number Packaging Price Buy
211370 5g $39.7 Buy
211370 25g $94.1 Buy
S0890 25g $29 Buy
S0890 250g $134 Buy
289072 100g $333 Buy

Sulfamide Chemical Properties,Uses,Production

Description

Sulfamide is a white solid substance that is normally produced by reacting sulfuryl chloride with ammonia. Sulfamide is stable under normal conditions and soluble in acetone and DMSO. Sulfamide may also refer to the functional group in organic chemistry, and it consists of at least one group attached to a nitrogen atom of sulfamide.
It is a carbonic anhydrase inhibitor and is widely used as a pharmaceutical intermediate.
Sulfamide is sensitive to moisture, thus should be kept away from water and humidity. It should also be stored away from oxidizing agents. Sulfamide should be kept in a tightly closed container and placed in a cool, dry, and well-ventilated condition.

Chemical Properties

White Solid

Uses

Similar to urea in many of its reactions, but is more acidic, and can act as a dibasic acid.

Uses

A carbonic anhydrase inhibitor; used for treatment of cancer.

Uses

Sulfamide and its derivatives can also be used to prepare fused thiadiazine systems, Reaction with 2-aminoacetophenones affords IH-2,1,3-benzothia- diazine 2,2-dioxides 77 (65JOC3960). The corresponding 3,4-dihydro deriv- atives are readily available from 2-aminobenzylamines with either sulfuryl chloride (70M1443) or sulfamide (66USP3278532; 71MI055). These kinds of compounds can also be obtained from N-aryl-N'-alkylsulfamides and s-trioxane in a reaction involving cyclization by intramolecular sulfamido- methylation (79JOC2032) (Scheme 30).

Definition

ChEBI: The simplest of the sulfamic acids consisting of a single sulfur atom covalently bound by single bonds to two amino groups and by double bonds to two oxygen atoms.

Purification Methods

Crystallise sulfamide from absolute EtOH. It decomposes at 250o. [Schenk in Handbook of Preparative Inorganic Chemistry (Ed. Brauer) Academic Press Vol I pp 482-483 1963.]

7791-25-5
7664-41-7
7803-58-9
Synthesis of Sulfamide from Sulfuryl chloride and Ammonia
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View Lastest Price from Sulfamide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Sulfamide pictures 2026-06-24 Sulfamide
7803-58-9
0.99 RongNa Biotechnology Co.,Ltd
Sulfamide pictures 2026-05-15 Sulfamide
7803-58-9
$825.00 25KG 99% 2000T Baoji Guokang Healthchem Co., Ltd.
Sulfamide pictures 2026-03-20 Sulfamide
7803-58-9
$100.00 1KG 99%min 20tons Hebei Chuanghai Biotechnology Co., Ltd
  • Sulfamide pictures
  • Sulfamide
    7803-58-9
  • 0.99
  • RongNa Biotechnology Co.,Ltd
  • Sulfamide pictures
  • Sulfamide
    7803-58-9
  • $825.00
  • 99%
  • Baoji Guokang Healthchem Co., Ltd.
  • Sulfamide pictures
  • Sulfamide
    7803-58-9
  • $100.00
  • 99%min
  • Hebei Chuanghai Biotechnology Co., Ltd
Sulfamamide sulfamide Sulfuryl amine SulfaMide, 98+% 5GR SulfaMid Sulphamide 99% Sulfamide purum, >=99.0% (N) [S(NH2)2O2] diamidodioxidosulfur Imidosulfamic acid (VAN) famide SULPHAMIDE SULFAMIDE RARECHEM AM UF NL01 LABOTEST-BB LT00077259 DIAMINO SULFONIC ACID sulphuric diamide Suleamide Sulfuryl amide Sulfamide, 98+% SULFAMIDE(4-HYDROXY-2-METHYL-2H-1,2-BENZOISOTHIAZOL-2-ACETICETHER-1,1-DIOXIDE) Sulfuryl amine Imidosulfamic Acid NSC 252 Sulfonyl Diamide Sulfuryl Diamide SULFAMIDE ( SULFURYL AMIDE ) Sulfamide > Sulfamide, 99%, for synthesis Famotidine Impurity 15 Sulfamide ISO 9001:2015 REACH Sulfamide (6CI, 8CI, 9CI, ACI) C16998170 Sulfamide Sulfonamide/Sulfamide SULFURIC DIAMIDE 7803-58-9 SO2NH22 NH22SO2 H4N2O2S Pharmaceutical intermediates Inhibitors Sulfur & Selenium Compounds Electronic Chemicals Micro/Nanoelectronics Others Starting Raw Materials & Intermediates Chemical Amines Famotidine Amines Inorganics