Contact us: +91 9550333722 040 - 40102781
Structured search
India
Choose your country
Different countries will display different contents
Try our best to find the right business for you.
My chemicalbook

Welcome back!

HomecompanyBenzonatate
Benzonatate
Benzonatate

Benzonatate

Price USD1.80
Packge 1KG
  • Min. Order:1g
  • Supply Ability:1kg/10kg/100kg
  • Time:2021-01-06

Product Details

  • Product NameBenzonatate
  • CAS No.104-31-4
  • EINECS No.203-194-7
  • MFC30H53NO11
  • MW603.74
  • AppearanceOilLight Yellow to Light Brown
  • Boiling point 649.0±55.0 °C(Predicted)
  • density 1.096±0.06 g/cm3(Predicted)
  • storage temp. Refrigerator, under inert atmosphere

Email: amy@coreychem.com 
Career Henan Chemical Co
Mob/Skype: +86-18317388371

Benzonatate Basic information
Product Name: Benzonatate
Synonyms: 4-(Butylamino)benzoicacid3,6,9,12,15,18,21,24,27-nonaoxao-ctacos-1-ylester;benzoicacid,4-(butylamino)-,3,6,9,12,15,18,21,24,27-nonaoxaoctacos-1-yles;benzononantin;benzononatine;tessalon;tessalon-ciba;thoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethylester;ventussin
CAS: 104-31-4
MF: C30H53NO11
MW: 603.74
EINECS: 203-194-7
Product Categories: Chemical Amines;Amines;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File: 104-31-4.mol
Benzonatate Structure
 
Benzonatate Chemical Properties
Boiling point  649.0±55.0 °C(Predicted)
density  1.096±0.06 g/cm3(Predicted)
pka 2.20±0.39(Predicted)
CAS DataBase Reference 104-31-4(CAS DataBase Reference)
 
Safety Information
Toxicity LD50 oral in mouse: 400mg/kg
MSDS Information
 
 
Benzonatate Usage And Synthesis
Originator Tessalon,Endo (Du Pont),US,1958
Uses Antitussive
Definition ChEBI: The ester obtained by formal condensation of 4-butylaminobenzoic acid with nonaethylene glycol monomethyl ether. Structurally related to procaine and benzocaine, it has an anaesthetic effect on the stretch sensors in the lungs, and is used as a non-narcoti cough suppressant.
Manufacturing Process 4.42 parts of para-butylamino-benzoic acid ethyl ester are put with 16.0 parts of a mixture of polyethylene glycol monomethyl ethers, boiling at 180°-220°C at a pressure of 0.01 mm of mercury, in a closed reaction vessel which is fitted with an adjustable inlet tube for solvents and a connection for distilling off in vacuo. In order to dry the mixture completely, it is heated for an hour at 100°-105°C and absolute xylene is introduced under the surface of the mixture in vacuo at a pressure of 12 mm of mercury. There is thus a constant stream of xylene steam passing through the whole apparatus, which removes the last traces of moisture and any other volatile impurities. The xylene is condensed in a cooler. The whole is cooled to 20°-30°C and 0.06 part of sodium methylate dissolved in 0.6 part of methanol is added.
Thereupon xylene is introduced again in vacuo at a temperature of 100°- 105°C whereby all the methanol and the ethanol formed during reesterification evaporates. The re-esterification is continued under these conditions until a specimen of the reaction mass is clearly soluble in cold water, which occurs after about 2-3 hours. There is now obtained in almost quantitative yield the ester of the formula wherein n stands for approximately 7 to 9, which still contains an excess of polyethylene glycol monomethyl ether. The ester is purified by dissolving in benzene and being washed several times with a sodium carbonate solution of 5% strength. It is advantageous to agitate all the washing solutions with fresh benzene. In this distribution between benzene and sodium carbonate solution the new ester remains in the benzene, the excess polyethylene glycol monomethyl ether and a small amount of brown impurities are taken up by the dilute soda solution. By evaporating the dried and filtered benzene solution there is obtained the new ester in the form of a colorless to very faintly yellow oil which is easily soluble in most organic solvents with the exception of aliphatic hydrocarbons. The new ester is precipitated from aqueous solutions when heated to about 42°C. but it dissolves again readily on cooling.
Brand name Tessalon (Forest).
Therapeutic Function Antitussive
Biological Functions Benzonatate (TessaIon) is related to the local anesthetic tetracaine. It anesthetizes the stretch receptors in the lungs, thereby reducing coughing.Adverse reactions include hypersensitivity, sedation, dizziness, and nausea.
 
Benzonatate Preparation Products And Raw materials

Company Profile Introduction

Technology research and transfer of pilot screening, pilot scale-up and mass production solutions , for pharmaceutical intermediates, biologicals and fine chemicals (Not including inflammable , explosive , hazardous goods ) ; Market : Nano material , metal catalyst , raw material of cosmetics , pharmaceutical intermediates , chemicals , photoelectric material , import and export of technology and goods (For projects subject to approval according to law, business activities can be carried out only after approval by relevant departments ).
  • Since:2020-12-17
  • Address: Room 702, Floor 7, Building 10, National University Science Park, High-Tech Zone, Zhengzhou City, He
INQUIRY