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CHLORPROPAMIDE

CHLORPROPAMIDE Structure
CAS No.
94-20-2
Chemical Name:
CHLORPROPAMIDE
Synonyms
p607;P-607;u-3818;u-9818;Adiaben;Asucrol;Catanil;Glisema;Meldian;Oradian
CBNumber:
CB8677954
Molecular Formula:
C10H13ClN2O3S
Molecular Weight:
276.74
MOL File:
94-20-2.mol
Modify Date:
2024/7/2 8:55:37

CHLORPROPAMIDE Properties

Melting point 128 °C
Boiling point 302°C (rough estimate)
Density 1.3046 (rough estimate)
refractive index 1.6300 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Sparingly), Methanol (Slightly)
form Solid
pka pKa 4.8 (Uncertain)
color White to Light Yellow
Water Solubility Soluble in ethanol (1:12), acetone (1:5), chloroform (1:9) and solutions of alkali hydroxides. Does not mix well with water.
Merck 14,2186
Stability Stable. Combustible.
CAS DataBase Reference 94-20-2(CAS DataBase Reference)
EPA Substance Registry System Chloropropamide (94-20-2)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08
Signal word  Warning
Hazard statements  H302-H361f-H373
Precautionary statements  P202-P260-P264-P270-P301+P312-P308+P313
Hazard Codes  Xn
Risk Statements  20/21/22-40
Safety Statements  22-36
WGK Germany  3
RTECS  YS6650000
HS Code  29350090
Toxicity LD50 i.p. in rats: 580 mg/kg (Goldenthal)
NFPA 704
0
3 0

CHLORPROPAMIDE price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) PHR1284 Chlorpropamide Pharmaceutical Secondary Standard; Certified Reference Material 94-20-2 1G ₹8107.93 2022-06-14 Buy
Sigma-Aldrich(India) C1290 Chlorpropamide analytical standard, ≥97% 94-20-2 25G ₹12221.43 2022-06-14 Buy
TCI Chemicals (India) C1220 1-(4-Chlorophenylsulfonyl)-3-propylurea 94-20-2 25G ₹4000 2022-05-26 Buy
Product number Packaging Price Buy
PHR1284 1G ₹8107.93 Buy
C1290 25G ₹12221.43 Buy
C1220 25G ₹4000 Buy

CHLORPROPAMIDE Chemical Properties,Uses,Production

Chemical Properties

white crystalline powder

Uses

Chlorpropamide is a sulfonylurea derivative. Chlorpropamide is a long acting hyopglycemic agent. Chlorpropamide is used in the treatment of diabetes metilus type 2. Chlorpropamide acts to increase the secretion of insulin and is not effective in patients who do not have pancreatic beta cell function.

Definition

ChEBI: An N-sulfonylurea that is urea in which a hydrogen attached to one of the nitrogens is substituted by 4-chlorobenzenesulfonyl group and a hydrogen attached to the other nitrogen is substituted by propyl group. Chlorpropamide is a hypogly aemic agent used in the treatment of type 2 (non-insulin-dependent) diabetes mellitus not responding to dietary modification.

General Description

Chlorpropamide is 4-chloro-N-[(propylamino)carbonyl]benzenesulfonamide; or 1-[(p-chlorophenyl)sulfonyl]-3-propylurea; or 1-(p-chlorobenzenesulfonyl)-3-propylurea(Diabinese, generic). The p-chlorophenyl moiety is quite resistantto P450-mediated hydroxylations; hence, blood levelsof the drug are sustained for a markedly long length of time,as aliphatic hydroxylation constitutes most of the clearance,and this happens relatively slowly. Although the -hydroxyland (ω–1)-hydroxyl metabolites (the latter formed in muchgreater portion) exert hypoglycemic potencies not much lessthan does the parent drug, elimination of these by conversion to the corresponding glucuronides occurs more rapidly thanhydroxylation of chlorpropamide, so blood levels of thesemetabolites remain low, and thus they probably do not makean appreciable contribution to the hypoglycemic action ofthis drug in clinical application. Removal of the entire propylside chain (oxidative N-dealkylation) also occurs to a significantextent (up to 20% of an orally administered dose), creatingthe inactive metabolite p-chlorobenzenesulfonylurea,about 10% of which degrades to the corresponding benzenesulfonamide.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

A halogenated 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).

Fire Hazard

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

Purification Methods

Crystallise the urea from aqueous EtOH. [Beilstein 11 IV 119.]

CHLORPROPAMIDE Preparation Products And Raw materials

Global( 256)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Kothari Phytochemicals and Industries Ltd. +91-9244448844 +91-9331023407 West Bengal, India 18 58 Inquiry
Quantum Drugs Chemicals +91 9443396658 +91 9362944455 Tamil Nadu, India 6 58 Inquiry
Medilink Pharmachem +91 (79) 3007-0133 New Delhi, India 424 50 Inquiry
OCEAN TRADING CORPORATION +91(22) 24921669 New Delhi, India 6211 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
SynZeal Research Pvt Ltd +1 226-802-2078 Gujarat, India 6522 58 Inquiry
Triveni chemicals 08048762458 New Delhi, India 6093 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
PNR Impex 07942548368 Mumbai, India 81 58 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
1-((p-chlorophenyl)sulfonyl)-3-propyl-ure 1-(p-Chlorophenylsulfonyl)-3-propylurea 1-Chloro-4-(([(propylamino)carbonyl]amino)sulfonyl)benzene 1-p-Chlorophenyl-3-(propylsulfonyl)urea 1-Propyl-3-(p-chlorobenzenesulfonyl)urea 4-Chloro-4-((propylamino)carbonyl)benzenesulfonamide 4-chloro-n-((propylamino)carbonyl)-benzenesulfonamid 4-chloro-n-[(propylamino)carbonyl]-benzenesulfonamid 4-chloro-n-[(propylamino)carbonyl]benzenesulfonamide 4-Chloro-N-[(propylamino)-carbonyl]benzenesulfonamide 4-Chloro-N-[(propylamino)carbonyl]benzene-sul-fonamide Adiaben Asucrol Benzenesulfonamide, 4-chloro-N-[(propylamino)carbonyl]- bioglumin Catanil Chlorodiabina Chloronase Chlorpropamid Clorpropamide Diabaril Diabechlor Diabenal Diabenese Diabeneza Diabetoral Diabet-pages diabexan Diabinese Diamel Ex Dynalase Glisema Hexathane Insulase Meldian Melitase Mellinese Millinese n-(4-chlorophenylsulfonyl)-n’-propylurea N-(4-Chlorophenylsulfonyl)-N'-propylurea n-(p-chlorobenzenesulfonyl)-n’-propylurea N-(p-Chlorobenzenesulfonyl)-N'-propylurea NCI-C01752 n-Propyl-N'-(p-chlorobenzenesulfonyl)urea n-propyl-n’-(p-chlorobenzenesulfonyl)urea n-propyl-n’-p-chlorphenylsulfonylcarbamide n-Propyl-N'-p-chlorophenylsulfonylcarbamide Oradian p607 P-607 prodiaben Stabinol u-3818 Chloropropamide USP CHLORPROPAMIDE USP 1-(p-chlorobenzenesulfonyl)-3-propylure CHLORPROPRAMIDE 4-chloro-N-(propylcarbamoyl)benzenesulfonamide