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Diazene, ethyl(1-methylethyl)-, also known as 1-ethyl-1,2-diazene or N-ethyl-N-(1-methylethyl)hydrazine, is an organic compound with the chemical formula C4H10N2. It is a colorless liquid with a strong, pungent odor and is highly flammable. Diazene, ethyl(1-methylethyl)- is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its potential health risks and environmental concerns, it is important to handle Diazene, ethyl(1-methylethyl)- with proper safety measures and in accordance with relevant regulations.

3896-18-2

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3896-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3896-18-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,9 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3896-18:
(6*3)+(5*8)+(4*9)+(3*6)+(2*1)+(1*8)=122
122 % 10 = 2
So 3896-18-2 is a valid CAS Registry Number.

3896-18-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl(propan-2-yl)diazene

1.2 Other means of identification

Product number -
Other names Ethanazo-1'-methylethan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3896-18-2 SDS

3896-18-2Downstream Products

3896-18-2Relevant academic research and scientific papers

Combination and Disproportionation Reactions of the Radical

Goergenyi, Miklos,Seres, Laszlo

, p. 1827 - 1830 (1991)

The radical (1) was produced in the di-tert-butyl peroxide-initiated and thermal decompositions of azoethane.Self-combination of 1 takes place almost exclusively at the carbon radical centre (1C).The disproportionation: combination ratio Δ(C2H5., 1N) ca. 0.38 (Δ = kd/kc) and the rate constant ratio kd(CH3., 1N)/kc(CH3., 1C) = 0.15 +/- 0.03.The cross-combination ratio Φ(CH3., 1C) = 1.38 +/- 0.11, which is lower than the cross-reaction ration Φ*(CH3., 1) ca. 2.5.

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