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Ethopabate

Ethopabate Suppliers list
Company Name: shandong perfect biotechnology co.ltd
Tel: +86-53169958659; +8618596095638
Email: sales@sdperfect.com
Products Intro: Product Name:Ethopabate
CAS:59-06-3
Purity:98% HPLC Package:1kg
Company Name: Hebei Mojin Biotechnology Co., Ltd
Tel: +8613288715578
Email: sales@hbmojin.com
Products Intro: Product Name:Ethopabate
CAS:59-06-3
Purity:99% Package:25KG
Company Name: Shaanxi TNJONE Pharmaceutical Co., Ltd
Tel: +8618740459177
Email: sarah@tnjone.com
Products Intro: Product Name:Ethopabate
CAS:59-06-3
Purity:99% Package:1kg
Company Name: Capot Chemical Co.,Ltd.
Tel: 571-85586718 +8613336195806
Email: sales@capotchem.com
Products Intro: Product Name:Methyl 4-acetamido-2-ethoxybenzoate
CAS:59-06-3
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: Nanjing ChemLin Chemical Industry Co., Ltd.
Tel: 025-83697070
Email: product@chemlin.com.cn
Products Intro: CAS:59-06-3
Purity:98% Package:g-Kg Remarks:White powder

Ethopabate manufacturers

  • Ethopabate
  • Ethopabate pictures
  • $0.00 / 1kg
  • 2024-04-11
  • CAS:59-06-3
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 1000kg
  • Ethopabate
  • Ethopabate pictures
  • $0.00 / 1kg
  • 2024-03-12
  • CAS:59-06-3
  • Min. Order: 1kg
  • Purity: 98% HPLC
  • Supply Ability: 100kg
  • Ethopabate
  • Ethopabate pictures
  • $0.00 / 1kg
  • 2023-09-26
  • CAS:59-06-3
  • Min. Order: 1kg
  • Purity: 98.00%
  • Supply Ability: 20tons
Ethopabate Basic information
Product Name:Ethopabate
Synonyms:Ethopabate, Vetranal;ETHOPABATE (4-ACETYLAMINO-2-ETHOXY-BENZOIC ACID METHYL ESTER);Ethopatate;Ethytpatate;ETHOPABATE;4-ACETYLAMINO-2-ETHOXY-BENZOIC ACID METHYL ESTER;METHYL 5-ACETAMIDO-2-ETHOXYBENZOATE (ETHOPABATE);Ethopabate, Methyl 4-acetamido-2-ethoxybenzoate
CAS:59-06-3
MF:C12H15NO4
MW:237.25
EINECS:200-414-3
Product Categories:NARDIL;animal pharmaceutical;Amines;Aromatics;Drug Analogues;Intermediates & Fine Chemicals;Pharmaceuticals;Aromatic Esters
Mol File:59-06-3.mol
Ethopabate Structure
Ethopabate Chemical Properties
Melting point 148-151 °C
Boiling point 426.1±35.0 °C(Predicted)
density 1.180±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility DMSO: 50 mg/mL (210.75 mM)
form A solid
pka14.12±0.70(Predicted)
Merck 13,3781
InChIInChI=1S/C12H15NO4/c1-4-17-11-7-9(13-8(2)14)5-6-10(11)12(15)16-3/h5-7H,4H2,1-3H3,(H,13,14)
InChIKeyGOVWOKSKFSBNGD-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC=C(NC(C)=O)C=C1OCC
CAS DataBase Reference59-06-3(CAS DataBase Reference)
EPA Substance Registry SystemEthopabate (59-06-3)
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
HS Code 2924296000
MSDS Information
ProviderLanguage
Ethopabate English
SigmaAldrich English
Ethopabate Usage And Synthesis
DescriptionEthopabate is a veterinary drug belonging to the class of antibiotics which contains an arylamide with a phenyl ring, a monocyclic aromatic hydrocarbon, and is a very safe drug used for the prophylaxis and treatment of coccidiosis in chickens. It has anticoccidial activity, especially against the intestinal form, and lacks activity against E. tenella of the cecum worm. The drug is a competitor of PABA, which is absorbed by the parasite and interferes with folate synthesis. It has good activity against E. acervulina and some strains of E. maxima and E. brunette. It is used only in combination with amprolium, first at a concentration of 4 ppm and later at a concentration of 40 ppm.This drug reaches peak activity on day 4 of the cycle.
Chemical PropertiesWhite to Off-White Solid
UsesA supplementary drug that improves the coccidiostatic effect of nicarbazin and amprolium in order to cure coccidiosis in chickens.
Usesantidepressant
DefinitionChEBI: Ethopabate is an amidobenzoic acid.
Clinical UseEthopabate is only a narrow anticoccidial spectrum drug against Eimeria acervulina. It has no or only slight activity against E. maxima, E. necatrix, E. tenella or E. brunetti. Today, ethopabate is applied only in combination with amprolium and sulfonamide.
Molecular InteractionsEthopabate is a 2-substituted PABA derivative (=4-acetamido-2-ethoxybenzoic acid methylester) and functions as a prodrug. Its activity becomes potentiated by pyrimethamine and antagonised by the simultaneous administration of PABA. Thus, the mode of action of ethopabate is similar to that of sulfonamides or sulfones.
Ethopabate Preparation Products And Raw materials
Raw materials3-Methyl-1-butanol
Preparation Products2-Ethoxy-4-amino-5-chlorobenzoic acid
Tag:Ethopabate(59-06-3) Related Product Information
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