Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Analytical Chemistry >  Standard >  Pharmaceutical Impurity Reference Standards >  ISOPROPAMIDE IODIDE

ISOPROPAMIDE IODIDE

Basic information Safety Supplier Related

ISOPROPAMIDE IODIDE Basic information

Product Name:
ISOPROPAMIDE IODIDE
Synonyms:
  • LABOTEST-BB LT00772055
  • ISOPROPAMIDE
  • ISOPROPAMIDE IODIDE
  • (3-carbamoyl-3,3-diphenylpropyl)diisopropylmethyl-ammoniuiodide
  • (3-carbamoyl-3,3-diphenylpropyl)diisopropylmethylammoniumiodide
  • 2,2-diphenyl-4-diisopropylaminobutyramidemethiodide
  • 5579md
  • darbid
CAS:
71-81-8
MF:
C23H33IN2O
MW:
480.43
EINECS:
200-766-8
Product Categories:
  • DARBID
Mol File:
71-81-8.mol
More
Less

ISOPROPAMIDE IODIDE Chemical Properties

Melting point:
199℃ (Decomposition)
Density 
1.2711 (estimate)
storage temp. 
Store at -20°C
solubility 
DMSO: 250 mg/mL (520.37 mM)
Water Solubility 
Practically insoluble in water
form 
powder to crystal
color 
White to Almost white
Merck 
14,5202
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
2
RTECS 
BP0693200
HS Code 
2924296000
Toxicity
LD50 oral in rat: > 10gm/kg

MSDS

More
Less

ISOPROPAMIDE IODIDE Usage And Synthesis

Originator

Darbid,SKF,US,1957

Uses

Isopropamide Iodide acts as an anticholinergic compound with inhibitory activity. Also acts as a muscarinic receptor antagonist which can be applied to treatment of diseases affecting cognition including Alzheimer’s disease.

Uses

Isopropamide inhibits muscarinic action of acetylcholine on postganglionic parasympathetic effector regions. It is used for treating stomach ulcers and inflamed intestine.

Definition

ChEBI: Isopropamide iodide is a diarylmethane.

Manufacturing Process

γ-Diisopropylamino-α,α-diphenylbutyronitrile (60 g) was added in several portions to a mixture of sulfuric acid (150 ml) and water (15 ml) and the solution was heated 3% hours on the steam bath and then poured on ice and made basic with NH4OH. The γ-diisopropylamino-α,α-diphenylbutyramide precipitated as a solid, which was taken up in methylene chloride from an aqueous slurry. The methylene chloride was separated and dried by filtering through anhydrous K2CO3. The solvent was removed by distillation, leaving the amide which was crystallized from Skellysolve B five times and found then to have MP 87.0° to 88.5°C.
γ-Diisopropylamino-α,α-diphenylbutyramide in propanol was refluxed 4 hours in the presence of excess methyl iodide. Upon dilution of the solution with ethyl acetate (100 ml per 50 ml isopropyl alcohol) and cooling γ- diisopropylamino-α,α-diphenylbutyramide methiodide precipitated, was collected by filtration and recrystallized (9.0 g) by dissolving in a hot mixtureof 100 ml isopropyl alcohol and 10 ml methanol and then diluting with 90 ml Skellysolve B, to give 8.3 g recrystallized product, MP 182° to 184°C.

brand name

Darbid (GlaxoSmithKline).

Therapeutic Function

Spasmolytic

General Description

Isopropamide iodide, 3-carbamoyl-3,3-diphenylpropyl)diisopropylmethylammoniumiodide (Darbid), occurs as a bitter, white to pale yellow, crystallinepowder that is only sparingly soluble in water butfreely soluble in chloroform and alcohol.
This drug, introduced in 1957, is a potent anticholinergic,producing atropine-like effects peripherally. Even with itsquaternary nature, it does not cause sympathetic blockade atthe ganglionic level except at high dosages. Its principal distinguishingfeature is its long duration of action. A singledose can provide antispasmodic and antisecretory effects foras long as 12 hours.

Clinical Use

ISOPROPAMIDE IODIDE is used as adjunctive therapy in the treatment of pepticulcer and other conditions of the GI tract associated withhypermotility and hyperacidity. It has the usual side effectsof anticholinergics (dryness of mouth, mydriasis, difficulturination) and is contraindicated in glaucoma, prostatic hypertrophy,etc.

Synthesis

Isopropamide, (3-carbamoyl-3,3-diphenylpropyl)di-iso-propylmethyl ammonium iodide (14.1.25), is synthesized by alkylating diphenylacetonitrile with di-isopropylaminoethylchloride in the presence of sodium amide, and the subsequent hydrolysis of the nitrile group of the resulting compound (14.1.23) to an amide group (14.1.24). Alkylation of this compound with methyliodide gives isopropamide (14.1.25) [19¨C22].

ISOPROPAMIDE IODIDESupplier

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Email
jkinfo@jkchemical.com
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Email
sj_scrc@sinopharm.com
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
TOKYO CHEMICAL INDUSTRY CO., LTD.
Tel
03-36680489
Email
Sales-JP@TCIchemicals.com