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Sulfamide

Sulfamide Suppliers list
Company Name: Hebei Mojin Biotechnology Co., Ltd
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CAS:7803-58-9
Purity:99% Package:25KG
Company Name: Hebei Yanxi Chemical Co., Ltd.
Tel: +8617531190177
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CAS:7803-58-9
Purity:0.99 Package:1kg;50USD Remarks:Factory direct sales
Company Name: airuikechemical co., ltd.
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CAS:7803-58-9
Purity:99.9% Package:1Kg;|5Kg;|25Kg
Company Name: Capot Chemical Co.,Ltd.
Tel: 571-85586718 +8613336195806
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Products Intro: Product Name:Sulfamide
CAS:7803-58-9
Purity:NLT 98% Package:1G;1KG;100KG
Company Name: Henan Tianfu Chemical Co.,Ltd.
Tel: +86-0371-55170693 +86-19937530512
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Products Intro: Product Name:Sulfamide
CAS:7803-58-9
Purity:99% Package:25KG;5KG;1KG

Sulfamide manufacturers

  • Sulfamide
  • Sulfamide pictures
  • $0.00 / 1Kg
  • 2024-03-26
  • CAS:7803-58-9
  • Min. Order: 1Kg
  • Purity: 99.9%
  • Supply Ability: 200tons
  • Sulfamide
  • Sulfamide pictures
  • $50.00 / 1kg
  • 2023-11-01
  • CAS:7803-58-9
  • Min. Order: 1kg
  • Purity: 0.99
  • Supply Ability: 10000
  • Sulfamide
  • Sulfamide pictures
  • $0.00 / 25KG
  • 2023-07-05
  • CAS:7803-58-9
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 50000KG/month
Sulfamide Basic information
Description
Product Name:Sulfamide
Synonyms:Sulfamamide;SulfaMide, 98+% 5GR;Sulphamide 99%;Sulfamide purum, >=99.0% (N);[S(NH2)2O2];diamidodioxidosulfur;Imidosulfamic acid (VAN);SULFAMIDE
CAS:7803-58-9
MF:H4N2O2S
MW:96.11
EINECS:232-262-9
Product Categories:Pharmaceutical intermediates;Inhibitors;Sulfur & Selenium Compounds;Electronic Chemicals;Micro/Nanoelectronics;Others;Starting Raw Materials & Intermediates;Chemical Amines;Famotidine;Amines;Inorganics
Mol File:7803-58-9.mol
Sulfamide Structure
Sulfamide Chemical 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
pka10.87±0.60(Predicted)
color White to practically white , free from visible impurities
PH5.67 at 21.7℃ and 10g/L
Water Solubility soluble
Sensitive Moisture Sensitive
Merck 14,8922
InChIKeyNVBFHJWHLNUMCV-UHFFFAOYSA-N
CAS DataBase Reference7803-58-9(CAS DataBase Reference)
NIST Chemistry ReferenceSulfamide(7803-58-9)
EPA Substance Registry SystemSulfamide (7803-58-9)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
9
TSCA Yes
HazardClass IRRITANT
HS Code 28530090
MSDS Information
ProviderLanguage
Sulfamide English
SigmaAldrich English
ACROS English
ALFA English
Sulfamide Usage And Synthesis
DescriptionSulfamide 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 PropertiesWhite Solid
UsesSimilar to urea in many of its reactions, but is more acidic, and can act as a dibasic acid.
UsesA carbonic anhydrase inhibitor; used for treatment of cancer.
UsesSulfamide 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).
DefinitionChEBI: 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 MethodsCrystallise 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.]
Tag:Sulfamide(7803-58-9) Related Product Information
Famotidine p-Toluenesulfonamide Sulfamethazine [3-[[[2-(DiaMinoMethyleneaMino)-4-thiazolyl]Methyl]thio]propionyl]sulfaMide Hydrochloride (FaMotidine IMpurity) FAMOTIDINE RELATED COMPOUND B 2-(4-(CHLOROMETHYL)THIAZOL-2-YL)GUANIDINE 3-[2-(Diaminomethyleneamino)-1,3-thiazol-4-ylmethylsulphinyl]-N-sulphamoyl propanamide Bis[(2-guanidino-4-thiazolyl)methyl]disulfide (S)-((2-Guanidino-4-thiazolyl)methylisothiourea dihydrochloride 3-Chloropropiononitrile 3-(2-Guanidino-thiazol-4-yl-methylthio)-propionitrile 3-(((2-GUANIDINO-4-THIAZOLYL)METHYL)THIO)PROPANIMIDC ACID METHYL ESTER 3-[2-(Diaminomethyleneamino)-1,3-thiazol-4-ylmethylsulphinyl]-N-sulphamoylpropanamidine FaMotidine Acid IMpurity 3-Hydroxypropionic acid N-DesaMinosulfonyl-N-cyano FaMotidine FaMotidine Acid IMpurity Methyl Ester 3-HYDROXYPROPIONAMIDE