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Home > Encyclopedia > Etofenamate

Etofenamate

pharmaceutical raw materials
Etofenamate structure

Etofenamate 

structure
  • CAS No:

    30544-47-9

  • Formula:

    C18H18F3NO4

  • Chemical Name:

    Etofenamate

  • Synonyms:

    Benzoic acid,2-[[3-(trifluoromethyl)phenyl]amino]-,2-(2-hydroxyethoxy)ethyl ester;Anthranilic acid,N-(α,α,α-trifluoro-m-tolyl)-,2-(2-hydroxyethoxy)ethyl ester;Etofenamate;Rheumon;2-(2-Hydroxyethoxy)ethyl flufenamate;Bay-d 1107;Glasel;B 577;Traumon Gel;Bayrogel;Rheumon gel;WHR 5020;TV 485;2-[[3-(Trifluoromethyl)phenyl]amino]benzoic acid 2-(2-hydroxyethoxy)ethyl ester;Reumon

  • Categories:

    Organic Chemistry  >  Amides

Description

Etofenamate is a non-steroidal anti-inflammatory drug used for the treatment joint and muscular pain.


2-[3-(trifluoromethyl)anilino]benzoic acid 2-(2-hydroxyethoxy)ethyl ester is a benzoate ester.|Etofenamate is used to treat muscle and joint paint. It is a non-steroidal anti-inflammatory drug (NSAID).

Etofenamate Basic Attributes

369.33

369.33

250-231-8

KZF0XM66JC

DTXSID2045448

M02AA06|M - Musculo-skeletal system

2922509090

Characteristics

67.8

4.7

1.3±0.1 g/cm3

<25 °C

132.5 °C

226.6±28.7 °C

1.552

Practically insoluble in water, miscible with ethanol (96 per cent) and with ethyl acetate.

Refrigerator

LD50 in male, female rats (mg/kg): 292, 470 orally; 140, 226 i.v.; 373, 397 i.p.; 643, 568 s.c. (Jacobi)

Safety Information

P264, P270, P273, P301+P310, P321, P330, P391, P405, P501

H301

|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P264, P270, P273, P301+P310, P321, P330, P391, P405, and P501|Aggregated GHS information provided by 28 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)

2-(2-hydroxyethoxy)-ethyl-N-(alpha,alpha,alpha-trifluoro- m-tolyl)anthranilate

Etofenamate Use and Manufacturing

Medication used to alleviate joint and muscle pain.

Computed Properties

Molecular Weight:369.3
XLogP3:4.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:9
Exact Mass:369.11879254
Monoisotopic Mass:369.11879254
Topological Polar Surface Area:67.8
Heavy Atom Count:26
Complexity:433
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Drug Function and Efficacy

It is a non-steroidal anti-inflammatory drug of the fenamic acid class that can inhibit cyclooxygenase and esteroxidase, thereby reducing the effects of prostaglandins and other inflammatory mediators, and exerting its anti-inflammatory and analgesic effects.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • Beijing Ansenbo Pharmaceutical Technology Co., Ltd.

    China China
    Active
  • Bayer Healthcare Company Ltd.

    China China
    Active
  • DUKE CHEM, S.A.U.

    European Union European Union
    Active

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