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2,3-Butanediol, dinitrate is an organic compound with the chemical formula C4H8N2O6. It is a nitrate ester derived from 2,3-butanediol, a four-carbon diol. 2,3-Butanediol, dinitrate is known for its explosive properties and is used in the production of certain types of explosives and propellants. It is also referred to as butanediolnitrat or BDN. Due to its potential hazards, handling and storage of 2,3-butanediol, dinitrate require strict safety measures to prevent accidents.

6423-45-6

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6423-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6423-45-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,2 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6423-45:
(6*6)+(5*4)+(4*2)+(3*3)+(2*4)+(1*5)=86
86 % 10 = 6
So 6423-45-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2O6/c1-3(11-5(7)8)4(2)12-6(9)10/h3-4H,1-2H3

6423-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitrooxybutan-2-yl nitrate

1.2 Other means of identification

Product number -
Other names 2,3-bis-nitrooxy-butane

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:6423-45-6 SDS

6423-45-6Downstream Products

6423-45-6Relevant academic research and scientific papers

Kinetics and Products of the Reactions of NO3 with Monoalkenes, Dialkenes, and Monoterpenes

Barnes, Ian,Bastian, Volker,Becker, Karl H.,Tong, Zhu

, p. 2413 - 2419 (2007/10/02)

Rate constants for the reactions of NO3 with a number of aliphatic mono- and dialkenes and monoterpenes have been determined in a 420 l reaction chamber at 1-bar total pressure of synthetic air by 298 K with a relative kinetic method.The products of these reactions have been investigated also at 1-bar total pressure of synthetic air with in situ FT-IR spectrometry and gas chromatography.In all cases, the initial formation of thermally unstable nitrooxy-peroxynitrate-type compounds containing the difunctional group -CH(OONO2)-CH(ONO2)- has been observed.The experimental results are consistent with a mechanism involving the formation of nitrooxy-alkoxy radicals, -CH(O)-CH(ONO2)-, via the self-reaction of the nitrooxy-peroxy radicals.The further reactions of the nitrooxy-alkoxy radicals then determine the final products.The main reaction pathways are (i) reaction with O2 to form nitrooxy-aldehydes or -ketones and HO2 and (II) thermal decomposition forming aldehydes/ketones and NO2.The mechanisms leading to the final products are discussed, and their possible relevance for the chemistry in the troposphere is considered.

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