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Octane-1,8-diyl dinitrate, also known as dinitrooctane, is an organic compound with the chemical formula C8H14N2O4. It is a yellow, oily liquid that is highly sensitive to shock and friction, making it a potential explosive. octane-1,8-diyl dinitrate is formed by the nitration of octane, where two nitro groups (-NO2) are introduced into the molecule at the 1st and 8th carbon positions. Octane-1,8-diyl dinitrate has been studied for its potential use as a high-energy fuel and as a component in propellants and explosives due to its high energy density. However, its sensitivity and handling challenges have limited its practical applications. It is important to note that due to its explosive nature, octane-1,8-diyl dinitrate requires careful and specialized handling, and is not suitable for unregulated or non-professional use.

3457-95-2

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3457-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3457-95-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,5 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3457-95:
(6*3)+(5*4)+(4*5)+(3*7)+(2*9)+(1*5)=102
102 % 10 = 2
So 3457-95-2 is a valid CAS Registry Number.

3457-95-2Upstream product

3457-95-2Downstream Products

3457-95-2Relevant academic research and scientific papers

The synthesis of alkane dinitrates and theirs efficiency for cetane improver

Siraprapakit, Songsom,Sangvanich, Polkit,Lertpratchya, Preecha,Pengprecha, Somchai

experimental part, p. 432 - 435 (2010/05/19)

Dinitrate compounds was prepared from alkane diols; 1,6-hexane diol, 1,8-octane diol, 1,10-decane diol, and 2-methyl-2,4-pentane diol using nitration reaction. These dinitrate compounds were used as cetane improver for diesel fuel. Results showed that the cetane number values has increased about 1 and 3 units for 0.05 and 0.10% by weight of dinitrate compounds, respectively, compared with base oil. Their efficiency is higher than commercial cetane improver, 2-ethylhexyl nitrate.

Separation of Diastereomeric and Enantiomeric Alkyl Nitrates - Systematic Approach to Chiral Discrimination on Cyclodextrin LIPODEX-D

Schneider, Manfred,Ballschmiter, Karlheinz

, p. 539 - 544 (2007/10/03)

High-resolution gas chromatographic separation of all diastereomeric monomethyl-substituted cyclohexyl nitrates is shown on a nonpolar methylpolysiloxane stationary phase, and the first application of this procedure to the environmental diastereomeric analysis of alkyl nitrates is presented.Two characteristic signals in the achiral analysis of atmospheric samples could be assigned to the smallest alkyl nitrate containing two asymmetric carbon atoms, 3-methyl-2-pentyl nitrate.Retention indices in the temperature-programmed separation based on the n-alkanes were determined.The homologous series of 1-alkyl nitrates were found to be useful as ECD-visible n-alkanes.Enantiomeric separation of alkyl nitrates was achieved on heptakis(3-O-acetyl,-2,6-di-O-pentyl)-β-cyclodextrin (LIPODEX-D).The influence of the nitrooxy group and the alkyl chain length on the chiral discrimination on LIPODEX-D is discussed for 25 chiral alkyl nitrates.The absolute configurations of some alkyl nitrates were assigned by asymmetric synthesis of enantiomerically pure references.The complexity of the alkyl nitrate mixtures present in air samoles does not allow a direct chiral separation as the alkyl nitrates partly coelute on the LIPODEX-D column.Column coupling of LIPODEX-D with a polar achiral stationary phase like polyalkylenglocol (PAG) was successfully applied to solve this problem, and the chiral alkyl nitrates present in a typical air sample were separated.A systematic nomenclature for alkyl nitrates is introduced to handle the steadily growing number of branched and long-chain nitrates detected in environmental analysis. - Keywords: analytical methods; alkyl nitrates; chiral resolution; cyclodextrins; gas chromatography

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