Valethamate bromide
Valethamate bromide Basic information
- Product Name:
- Valethamate bromide
- Synonyms:
-
- S 78
- Valeric acid, 3-methyl-2-phenyl-, ester with diethyl(2-hydroxyethyl)methylammonium bromide
- Velamate
- ethanaminium bromide
- N,N-Diethyl-N-methyl-2-((3-methyl-2-phenylpentanoyl)
- Diethyl-methyl-[2-(3-methyl-2-phenyl-pentanoyl)oxyethyl]azanium bromide
- N,N-Diethyl-N-methyl-2-[(3-methyl-1-oxo-2-phenylpentyl)oxy]ethanaminium Bromide N-[2-(2-Methyl-1-phenylbutylcarbonyloxy)ethyl]diethylmethylammonium Bromide
- N,N-Diethyl-N-Methyl-2-((3-Methyl-2-phenylpentanoyl)oxy)ethanaMiniuM broMide
- CAS:
- 90-22-2
- MF:
- C19H32BrNO2
- MW:
- 386.37
- EINECS:
- 201-977-8
- Product Categories:
-
- Ammonium Bromides (Quaternary)
- Quaternary Ammonium Compounds
- Mol File:
- 90-22-2.mol
Valethamate bromide Chemical Properties
- Melting point:
- 120-127℃
- RTECS
- BP7600000
- storage temp.
- Inert atmosphere,Room Temperature
- Water Solubility
- almost transparency in Water
- solubility
- DMSO : 100 mg/mL (258.82 mM; Need ultrasonic)
- form
- Powder
- color
- White to Almost white
- Merck
- 14,9906
- CAS DataBase Reference
- 90-22-2(CAS DataBase Reference)
MSDS
- Language:English Provider:Valethamate bromide
Valethamate bromide Usage And Synthesis
Originator
Murel,Ayerst,US
Definition
ChEBI: Valethamate bromide is an alkylbenzene.
Manufacturing Process
Benzyl cyanide is first reacted with 2-butylbromide in the presence of sodium amide to give 2-phenyl-3-methylvaleronitrile which is hydrolyzed by sulfuric acid to give 3-methyl-2-phenylpentanoic acid. 24 g of 2-phenyl-3- methylpentanoic acid are heated for one hour at 175° to 185°C with 30 g of 2-diethylaminoethanol and 0.5 g of sodium methylate. The excess diethylaminoethanol is removed in vacuo, the residue is dissolved in 300 cc of 2 N-acetic acid, the acid solution is shaken with ether and made alkaline with concentrated potassium carbonate solution and ice. The ether solution is washed with water, dried with sodium sulfate and evaporated. The residue is distilled under high vacuum, yielding 20 to 21 g of the basic ester (60% of the theoretical) is obtained, the ester boiling at 98° to 100°C at a pressure of 0.03 mm. The hydrochloride of the ester melts at 112°to 113°C and the methobromide at 100° to 101°C.
Therapeutic Function
Anticholinergic
Safety Profile
Poison by ingestion, subcutaneous, and intravenous routes. See also ESTERS and BROMIDES. When heated to decomposition it emits very toxic fumes of NOx, NH3, and Br-.
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Valethamate bromide(90-22-2)Related Product Information
- Otilonium bromide
- Diphenyldimethoxysilane
- Ammonium chloride
- Sodium bromate
- Benzyldodecyldimethylammonium bromide
- Diethyl phthalate
- Pipecuronium bromide
- p-(2-Methoxyethyl) phenol
- Rocuronium bromide
- 4-Methoxyphenylacetone
- Tiotropium bromide
- Molybdic acid
- Tetraethylammonium bromide
- Phenyltriethoxysilane
- Ethidium bromide
- Mefenpyr-diethyl
- Ipratropium bromide monohydrate
- Ammonium sulfate