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Fomocaine

CAS No.
17692-39-6
Chemical Name:
Fomocaine
Synonyms
P-652;Panacain;fomocain;Fomocaine;p-Fomocaine;4-(3-(4-(PHENOXYMETHYL)PHENYL)PROPYL)MORPHOLINE;Morpholine, 4-[3-[4-(phenoxymethyl)phenyl]propyl]-
CBNumber:
CB11178806
Molecular Formula:
C20H25NO2
Molecular Weight:
311.42
MDL Number:
MFCD00074897
MOL File:
17692-39-6.mol
Last updated:2023-05-04 17:34:34

Fomocaine Properties

Melting point 52-53°
Boiling point bp1.1 238-240°
Density 1.0899 (rough estimate)
refractive index 1.5614 (estimate)
pka 7.44±0.10(Predicted)
color Crystals from pet ether
FDA UNII 4XO7A09HQM

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS07,GHS05,GHS09
Signal word  Danger
Hazard statements  H317-H318-H302-H400
Precautionary statements  P280-P305+P351+P338-P310-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501-P273-P391-P501-P264-P270-P301+P312-P330-P501
Toxicity LD50 i.v. in mice: 175 mg/kg (Nieschulz)

Fomocaine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich R277762 FOMOCAINE AldrichCPR 17692-39-6 250MG $110 2024-03-01 Buy
Product number Packaging Price Buy
R277762 250MG $110 Buy

Fomocaine Chemical Properties,Uses,Production

Originator

Erbocain,Heilit,W. Germany,1967

Definition

ChEBI: Fomocaine is an amine.

Manufacturing Process

64 parts of dry sodium phenolate are dissolved in 300 parts of methylisobutyl ketone by heating at 110°C. 103 parts of γ-(4-chloromethylphenyl)propyl chloride are added dropwise with agitation, and the mixture is maintained at 110°C for a period of 4 hours with constant agitation. After cooling, the reaction mixture is washed 2 or 3 times with 100 parts of water and the methylisobutyl ketone is distilled off under reduced pressure. The residue is taken up in 200 parts of petroleum ether and γ-(4-phenoxymethylphenyl) propyl chloride is crystallized by addition of ice water. The crystals are filtered off employing a suction pump and dried at 100°C in vacuo (10 mm Hg) for 1 to 2 hours. The γ-(4-phenoxymethylphenyl)propyl chloride melts at 55°C to 56°C after recrystallization from petroleum ether.
130 parts of γ-(4-phenoxymethylphenyl)propyl chloride are heated under reflux at 140°C for 24 hours with 130 parts of morpholine. The reaction mixture is treated to give N-[(γ-phenoxymethylphenyl)propyl]-morpholine, which forms colorless crystals melting at 52°C to 53°C when crystallized from n-heptane.

Therapeutic Function

Local anesthetic

Safety Profile

Poison by intravenous and intraperitoneal routes. Moderately toxic by subcutaneous route. When heated to decomposition it emits toxic fumes of NOx.

Fomocaine Preparation Products And Raw materials

Raw materials

Preparation Products

Fomocaine Suppliers

Global( 5)Suppliers
Supplier Tel Email Country ProdList Advantage
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
Supplier Advantage
Alchem Pharmtech,Inc.
58

17692-39-6(Fomocaine)Related Search:

Fomocaine fomocain 4-(3-(4-(PHENOXYMETHYL)PHENYL)PROPYL)MORPHOLINE P-652 Panacain p-Fomocaine Morpholine, 4-[3-[4-(phenoxymethyl)phenyl]propyl]- 17692-39-6