18413-14-4

Basic information

• Product Name: ethylhydrazine
• Synonyms: 1-Ethylhydrazine hydrochloride;Hydrazine, ethyl-, Monohydrochloride;ethylhydrazine hydrochloride
• CAS NO: 18413-14-4
• Molecular Formula: C₂H₈N₂*ClH
• Molecular Weight: 96.58
• Mol File: 18413-14-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 107.9°Cat760mmHg
• Flash Point: 15.7°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 26.6mmHg at 25°C
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: ethylhydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: ethylhydrazine(18413-14-4)
• EPA Substance Registry System: ethylhydrazine(18413-14-4)

Safety Data

• Hazardous Substances Data: 18413-14-4(Hazardous Substances Data)

Usage

Description

Ethylhydrazine is a highly reactive and potentially dangerous chemical compound, characterized by its clear, colorless liquid form and an ammonia-like odor. It is recognized as a strong reducing agent and is known for its high toxicity to humans, which can result in skin and eye irritation, respiratory issues, and even cancer with prolonged exposure. Due to its hazardous nature, ethylhydrazine requires careful handling, the use of personal protective equipment, and strict adherence to safety guidelines for storage and disposal to prevent harm to both humans and the environment.

Uses

Used in Laboratory Applications:
Ethylhydrazine is used as a laboratory reagent for various chemical reactions and experiments due to its strong reducing properties.
Used in Aerospace Industry:
In the aerospace industry, ethylhydrazine is utilized as a rocket propellant, capitalizing on its high reactivity to produce the necessary thrust for space missions.

InChI:InChI=1/C2H8N2.ClH/c1-2-4-3;/h4H,2-3H2,1H3;1H

Upstream product

• 2386-64-3 ethylmagnesium chloride 

Downstream Products

• 17629-26-4 1-ethyl-3,5-dimethylpyrazole 
• 1622077-65-9 ethyl 1-ethyl-5-phenyl-4,5-dihydro-1H-pyrazole-3-carboxylate 
• 7422-99-3 1-ethyl-2-(propan-2-ylidene)hydrazine 
• 1345507-91-6 C₁₂H₁₁N₃O₂ 
• 152713-69-4 5-Butyl-4-(2'-cyano-biphenyl-4-ylmethyl)-2-ethyl-2H-pyrazole-3-carboxylic acid ethyl ester 
• 1142400-25-6 C₁₁H₁₂Cl₂N₄ 

Related news

Coordination compounds of ethylhydrazine (cas 18413-14-4) and 2,2,2-Trifluoroethylhydrazine (cas 18413-14-4); crystal and molecular structure of dichlorotetrakis(2,2,2-Trifluoroethylhydrazine (cas 18413-14-4)) nickel(II)09/03/2019

Ethylhydrazine (EH) forms the complexes MX2(EH)2 (M = Co, Ni; X = Cl; M = Co, X = Br), NiBr2(EH)2(H2O) and MX2(EH) (M = Zn, Cd; X = Cl; M = Zn, X = Br). Spectroscopic evidence suggests that these all contain bridging hydrazine ligands, the cobalt and nickel complexes containing six coordinated m...detailed

Spin-trapping of free radicals formed during microsomal metabolism of ethylhydrazine (cas 18413-14-4) and acetylhydrazine09/02/2019

Radicals formed during oxidative metabolism of ethylhydrazine have been spin-trapped with PBN1. The trapped species has been identified as an ethyl radical by comparison of the ESR parameters of the PBN-adduct with (1) those of the analogous adduct formed during CuCl2-catalyzed oxidation of ethy...detailed

Relevant articles and documents

Reactions of grignard reagents with nitrous oxide

The chemical activation of nitrous oxide (N2O) can be achieved by organocalcium, organosodium, and organolithium compounds. Grignard reagents, on the other hand, are believed to be inert. We demonstrate that this generalization is not correct. Some aliphatic Grignard reagents undergo a rapid conversion when subjected to an atmosphere of N2O. Hydrazones are the main reaction products.