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Acetohexamid

ACETOHEXAMIDE Struktur
968-81-0
CAS-Nr.
968-81-0
Bezeichnung:
Acetohexamid
Englisch Name:
ACETOHEXAMIDE
Synonyma:
dymelor;Cyclamide;u14812;u-14812;dimelin;dimelor;minoral;ordimel;tsiklamid;DiMelor-d6
CBNumber:
CB1316029
Summenformel:
C15H20N2O4S
Molgewicht:
324.4
MOL-Datei:
968-81-0.mol

Acetohexamid Eigenschaften

Schmelzpunkt:
188-190° (GB 912789); mp 175-177° (Marshall)
Dichte
1.2528 (rough estimate)
Brechungsindex
1.6930 (estimate)
storage temp. 
Refrigerator
L?slichkeit
DMSO: ~45 mg/mL
Aggregatzustand
solid
pka
4.32±0.10(Predicted)
Farbe
white
Wasserl?slichkeit
0.25g/L(25 ºC)
Major Application
forensics and toxicology
pharmaceutical (small molecule)
InChI
1S/C15H20N2O4S/c1-11(18)12-7-9-14(10-8-12)22(20,21)17-15(19)16-13-5-3-2-4-6-13/h7-10,13H,2-6H2,1H3,(H2,16,17,19)
InChIKey
VGZSUPCWNCWDAN-UHFFFAOYSA-N
SMILES
CC(=O)c1ccc(cc1)S(=O)(=O)NC(=O)NC2CCCCC2
CAS Datenbank
968-81-0
EPA chemische Informationen
Acetohexamide (968-81-0)

Sicherheit

S-S?tze: 36
WGK Germany  2
RTECS-Nr. YR7350000
TSCA  TSCA listed
Speicherklasse 11 - Combustible Solids
Giftige Stoffe Daten 968-81-0(Hazardous Substances Data)
Toxizit?t LD50 oral in rat: > 2gm/kg

Acetohexamid Chemische Eigenschaften,Einsatz,Produktion Methoden

S-S?tze Betriebsanweisung:

S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.

Verwenden

Acetohexamide is a sulfonylurea derivative. Acetohexamide is a hyopglycemic agent with moderate uricosuric activity. Acetohexamide is a first generation medication used in the treatment of diabetes metilus type 2.

Definition

ChEBI: An N-sulfonylurea that is urea in which a hydrogen attached to one of the nitrogens is replaced by a p-acetylphenylsulfonyl group, while a hydrogen attached to the other nitrogen is replaced by a cyclohexyl group.

Allgemeine Beschreibung

Acetohexamide is 4-acetyl-N-[(cyclohexylamino)carbonyl]benzenesulfonamide; or 1-[(p-acetylphenyl)sulfonyl]-3-cyclohexylurea; or 1-(p-acetylbenzenesulfonyl)-3-cyclohexylurea(generic). Acetohexamide incorporates the nearly optimal(for potency) cyclohexyl moiety in the “right-hand” sideof its molecular structure, but a p-acetyl substituent on the“l(fā)eft-side” benzene ring that decreases lipophilicity and israpidly biotransformed by reduction to an active metabolitethat is cleared relatively rapidly (see preceding discussion) independentlyof any P450s.

Air & Water Reaktionen

Water insoluble.

Reaktivit?t anzeigen

An amide. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Brandgefahr

Flash point data for ACETOHEXAMIDE are not available; however, ACETOHEXAMIDE is probably combustible.

Clinical Use

Acetohexamide is metabolized in the liver to a reducedform, the α -hydroxyethyl derivative. This metabolite, themain one in humans, possesses hypoglycemic activity.Acetohexamide is intermediate between tolbutamide andchlorpropamide in potency and duration of effect on bloodsugar levels.

Sicherheitsprofil

Human reproductive effects by an unspecified route: stillbirth. Mildly toxic by ingestion. When heated to decomposition it emits very toxic fumes of SO, and NOx,.

Acetohexamid Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Acetohexamid Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 107)Lieferanten
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Aladdin Scientific

tp@aladdinsci.com United States 57505 58

968-81-0(Acetohexamid)Verwandte Suche:


  • 4-ACETYL-N-[(CYCLOHEXYLAMINO)-CARBONYL]BENZENESULFONAMIDE
  • ACETOHEXAMIDE
  • u-14812
  • ACETOHEXAMIDE, USP GRADE ORAL HYPOGLYCEM IC AGE
  • 1-(p-acetylbenzenesulfonyl)-3-cyclohexylure
  • 1-(4-acetylphenyl)sulfonyl-3-cyclohexylurea
  • 1-(4-acetylphenyl)sulfonyl-3-cyclohexyl-urea
  • 1-cyclohexyl-3-(4-ethanoylphenyl)sulfonyl-urea
  • Acetohexamide (250 mg)
  • BenzenesulfonaMide, 4-acetyl-N-[(cyclohexylaMino)carbonyl]-
  • 1-[(p-Acetylphenyl)su
  • 1-(p-Acetylbenzenesulfonyl)
  • 4-Acetyl-N-[(cyclohexyl-d6-aMino)carbonyl]benzenesulfonaMide
  • AcetohexaMide-d6
  • -d6 DiMelin-d6
  • DiMelor-d6
  • DyMelor-d6
  • GaMadiabet-d6
  • Hypoglicil-d6
  • Metaglucina-d6
  • Minoral-d6
  • OrdiMel-d6
  • TsiklaMid-d6
  • U 14812-d6
  • 1-((p-acetylphenyl)sulfonyl)-3-cyclohexyl-ure
  • 1-((p-acetylphenyl)sulfonyl)-3-cyclohexylurea
  • 1-(p-acetylbenzenesulfonyl)-3-cyclohexylurea
  • 4-acetyl-n-((cyclohexylamino)carbonyl)-benzenesulfonamid
  • 4-acetyl-n-[(cyclohexylamino)carbonyl]-benzenesulfonamid
  • 4-acetyl-n-benzenesulfonamide
  • acetohexamid
  • dimelin
  • dimelor
  • gamadiaber
  • gamadiabet
  • hypoglicil
  • metaglucina
  • minoral
  • n-(p-acetylphenylsulfonyl)-n’-cyclohexylurea
  • nci-c03247
  • ordimel
  • tsiklamid
  • u14812
  • ACETOHEXAMIDE USP/EP/BP
  • Acetoexamide
  • Acetohexamide (1006007)
  • Cyclamide
  • dymelor
  • inhibit,Inhibitor,Acetohexamide
  • Acetohexamide, 10 mM in DMSO
  • 1-[(paraethylacylbenzene)sulfonylacyl]-3-cyclohexylurea
  • Acetohexamide (Standard)
  • 968-81-0
  • C15H20N2O4S
  • AA to AL
  • Alphabetic
  • Analytical Chromatography Product Catalog
  • Analytical Standards
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