56795-65-4

Basic information

• Product Name: BUTYLHYDRAZINE HYDROCHLORIDE
• Synonyms: butyl-hydrazinhydrochloride;BUTYLHYDRAZINE HYDROCHLORIDE;1-ButylhydrazineHCl;1-Butylhydrazinehydrochloride;Ccris 1291;Hydrazine, butyl-, hydrochloride;N-Butylhydrazine hydrochloride
• CAS NO: 56795-65-4
• Molecular Formula: C₄H₁₂N₂*ClH
• Molecular Weight: 124.61
• Mol File: 56795-65-4.mol
• Article Data: 3

Chemical Properties

• Melting Point: 149-154℃
• Boiling Point: 152.4°Cat760mmHg
• Flash Point: 48.6°C
• Appearance: /
• Density: 0.823g/cm³
• Vapor Pressure: 3.5mmHg at 25°C
• CAS DataBase Reference: BUTYLHYDRAZINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: BUTYLHYDRAZINE HYDROCHLORIDE(56795-65-4)
• EPA Substance Registry System: BUTYLHYDRAZINE HYDROCHLORIDE(56795-65-4)

Safety Data

• Hazardous Substances Data: 56795-65-4(Hazardous Substances Data)

Usage

Uses

Butylhydrazine can be used in the refining of hydrocarbon gases for removal of trace aldehydes.

InChI:InChI=1/C4H12N2.ClH/c1-2-3-4-6-5;/h6H,2-5H2,1H3;1H

Upstream product

• 149268-06-4 N'-butylhydrazinecarboxylic acid tert-butyl ester 

Downstream Products

• 3524-35-4 1-butyl-3-methyl-1H-pyrazol-5-amine 
• 52709-73-6 L-butoxycarbonylhydrazine 
• 1451838-05-3 butyl-N-benzoylhydrazine 

Relevant articles and documents

Synthesis method for pharmaceutically acceptable salt of alkylhydrazine

The invention discloses a synthesis method for pharmaceutically acceptable salt of alkylhydrazine. According to the method, with hydrazine hydrate and BOC anhydride as starting raw materials, BOC hydrazine is synthesized firstly, then alkyl compounds are added in, BOC alkylhydrazine is obtained, finally BOC is removed, and the pharmaceutically acceptable salt of the corresponding alkylhydrazine is obtained in a conversion manner. According to the synthesis method, the raw materials for use are low in price and cost and easy to obtain. The synthesis method is short in synthesis route and high in yield, the obtained product is high in chemical purity, special production equipment is not needed for all reactions, and obtained intermediates and the final product do not need column chromatography and crystallization and purification.

1,1,4,4,-TETRAALKYLAMIDAZINES. SYNTHESIS OF MONOALKYLHYDRAZINES

A series of 1,1,4,4,-tetraalkylamidazines were synthesized.Their IR, UV, and 1H and 13C NMR spectra were investigated, and the characteristics of their stereochemical structure are discussed.Amidazines are alkylated by the action of alkyl iodides at the imine nitrogen atom.Alkaline cleavage of the alkyl iodide derivatives is a method for the production of monoalkylhydrazines.