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Tolazamid

TOLAZAMIDE Struktur
1156-19-0
CAS-Nr.
1156-19-0
Bezeichnung:
Tolazamid
Englisch Name:
TOLAZAMIDE
Synonyma:
U-17835;diabewas;tolanase;tolinase;Tolonase;norglycin;nsc-70762;olazamide;nci-c03327;TOLAZAMIDE
CBNumber:
CB9355686
Summenformel:
C14H21N3O3S
Molgewicht:
311.4
MOL-Datei:
1156-19-0.mol

Tolazamid Eigenschaften

Schmelzpunkt:
162-164°C
Siedepunkt:
300°C (rough estimate)
Dichte
1.2228 (rough estimate)
Brechungsindex
1.6740 (estimate)
storage temp. 
Sealed in dry,Room Temperature
L?slichkeit
Very slightly soluble in water; freely soluble in chloroform; soluble in acetone; slightly soluble in ethanol (96%).
Aggregatzustand
Solid
pka
3.6(at 25℃)
Farbe
White to Off-White
Wasserl?slichkeit
65.4mg/L(30 ºC)
CAS Datenbank
1156-19-0(CAS DataBase Reference)
EPA chemische Informationen
Tolazamide (1156-19-0)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher Xn
R-S?tze: 22
S-S?tze: 36
WGK Germany  3
RTECS-Nr. YT4400000
HS Code  2935904000
Giftige Stoffe Daten 1156-19-0(Hazardous Substances Data)
Toxizit?t LD50 in rats, mice (mg/kg): >5000 orally, 2239 i.p. (Dulin)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H370 Sch?digt die Organe. Spezifische Zielorgan-Toxizit?t (einmalige Exposition) Kategorie 1 Achtung GHS hazard pictogramssrc="/GHS08.jpg" width="20" height="20" /> P260, P264, P270, P307+P311, P321,P405, P501
Sicherheit
P260 Dampf/Aerosol/Nebel nicht einatmen.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P307+P311 BEI Exposition: GIFTINFORMATIONSZENTRUM oder Arzt anrufen.
P321 Besondere Behandlung
P405 Unter Verschluss aufbewahren.
P501 Inhalt/Beh?lter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

Tolazamid Chemische Eigenschaften,Einsatz,Produktion Methoden

R-S?tze Betriebsanweisung:

R22:Gesundheitssch?dlich beim Verschlucken.

S-S?tze Betriebsanweisung:

S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.

Beschreibung

Tolazamide is a first generation sulfonylurea that inhibits sulfonylurea receptor 1 (SUR1) linked to the inwardly rectifying potassium channel (KIR6.2; IC50 = 4.2 μM in HEK293 cells transfected with the human receptor). It has no effect on glucose uptake in L6 rat skeletal muscle cells when used at a concentration of 0.6 mg/mL but enhances glucose uptake two-fold when used in combination with insulin. In vivo, tolazamide (128 mg/kg) reduces glomerulosclerosis and albumin excretion in a rat model of insulin-dependent diabetes induced by streptozotocin . Formulations containing tolazamide have been used in the treatment of type 2 diabetes.

Chemische Eigenschaften

White Solid

Verwenden

Labelled Tolazamide, an antidiabetic.

Definition

ChEBI: An N-sulfonylurea that is 1-tosylurea in which a hydrogen attached to the nitrogen at position 3 is replaced by an azepan-1-yl group. A hypoglycemic agent, it is used for the treatment of type 2 diabetes mellitus.

Allgemeine Beschreibung

Tolazamide is N-[[(hexahydro-1H-azepin-1-yl)amino]carbonyl]-4-methylbenzenesulfonamide; or 1-(hexahydro-1H-azepin-1-yl)-3-(p-tolylsulfonyl)urea; or 1-(4-methylphenylsulfonyl)-3-(hexahydro-1H-azepin-1-yl)urea (generic).Tolazamide incorporates a fully saturated azepine moietythat is but weakly basic, with a pKa of~3.32 The pKa of thesulfonylurea group lies within the typical range; thus, inareas of the duodenum wherein the pH falls within the rangeof 4 to 5, the uncharged form of the drug is the predominantspecies, and its lipophilicity lends to rapid absorption bypassive diffusion.

Air & Water Reaktionen

TOLAZAMIDE may be sensitive to prolonged exposure to air. Insoluble in water.

Reaktivit?t anzeigen

TOLAZAMIDE is an amide. 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). TOLAZAMIDE is incompatible with acids. .

Brandgefahr

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

Tolazamid Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Tolazamid Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 145)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Shaanxi Dideu Medichem Co. Ltd
+86-29-81148696 +86-15536356810
1022@dideu.com China 3882 58
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795
ivan@atkchemical.com China 32956 60
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28172 58
Hubei xin bonus chemical co. LTD
86-13657291602
linda@hubeijusheng.com CHINA 22963 58
career henan chemical co
+86-0371-86658258 +8613203830695
factory@coreychem.com China 29810 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000
marketing@targetmol.com United States 32161 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763
sales@tnjchem.com China 34563 58
HANGZHOU CLAP TECHNOLOGY CO.,LTD
86-571-88216897,88216896 13588875226
sales@hzclap.com CHINA 6312 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471
sales@sarms4muscle.com China 10473 58
Labnetwork lnc.
+86-27-50766799 +8618062016861
contact@labnetwork.com China 19987 58

1156-19-0(Tolazamid)Verwandte Suche:


  • 1-(hexahydro-1-azepinyl)-3-p-tolylsulfonylurea
  • 1-(hexahydro-1h-azepin-1-yl)-3-(p-tolylsulfonyl)-ure
  • 1-(hexahydro-1h-azepin-1-yl)-3-(p-tolylsulfonyl)urea
  • 4-(p-tolylsulfonyl)-1,1-hexamethylenesemicarbazide
  • Tolazamide Solution, 100ppm
  • diabewas
  • n-(((hexahydro-1h-azepin-1-yl)-amino)carbonyl)-4-methyl-benzenesulfonamid
  • n-(p-toluenesulfonyl)-n’-hexamethyleniminourea
  • n,((hexahydro-1h-azepin-1-yl)amino)carbonyl)-4-methyl-benzenesulfonamid
  • n-[[(hexahydro-1h-azepin-1-yl)-amino]carbonyl]-4-methylbenzenesulfonamide
  • nci-c03327
  • norglycin
  • nsc-70762
  • tolanase
  • tolazolamide
  • tolinase
  • SALOR-INT L254916-1EA
  • N-[[(HEXAHYDRO-1H-AZEPINYL)AMINO]CARBONYL]-4-METHYLBENZENESULFONAMIDE
  • U-17835
  • TOLAZAMIDE
  • LABOTEST-BB LT00772329
  • 1-[HEXAHYDRO-1H-AZEPIN-1-YL]-3-[P-TOLUENESULFONYL]UREA
  • Tolonase
  • Tolazamide (200 mg)
  • TOLAZAMIDE;NSC 70762
  • 1-(4-Methylphenylsulfonyl)-3-(hexahydro-1H-azepin-1-yl)urea
  • Benzenesulfonamide, N-[[(hexahydro-1H-azepin-1-yl)amino]carbonyl]-4-methyl-
  • Tolbutamide EP Impurity C
  • Tolbutamide Impurity 3 (Tolbutamide EP Impurity C)
  • TOLAZAMIDE USP/EP/BP
  • 1-(azepan-1-yl)-3-(4-methylbenzenesulfonyl)urea
  • 1-(azepan-1-yl)-3-(4-methylphenyl)sulfonylurea
  • Tolazamide (1668001)
  • BRN 2938799
  • BRN-2938799
  • 4-chloro-3-[5-(2-hydroxyphenyl)-4,5-dihydro-1H-pyrazol-7-yl]phenol
  • N-(Azepan-1-ylcarbamoyl)-4-methylbenzenesulfonamide
  • 1-azepan-1-yl-3-[(4-methylphenyl)sulfonyl]urea (tolazamide)
  • olazamide
  • Tolbutamide Impurity C
  • 1156-19-0
  • C14H21N3O3S
  • Stimulates pancreatic islet cells to secrete insulin; blocks ATP-sensitive K+ channels.
  • Cell Signaling and Neuroscience
  • Cell Biology
  • BioChemical
  • Voltage-gated Ion Channels
  • Potassium Channel Modulators
  • Ion Channels
  • Monovalent Ion Channels
  • Amines
  • Aromatics
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Sulfur & Selenium Compounds
  • TOLINASE
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