nitroalkane


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Related to nitroalkane: Nitro functional group

nitroalkane

[¦nī·trō′al‚kān]
(organic chemistry)
References in periodicals archive ?
4) Aldehydes 1,5-Pentanediol (Glutaraldehyde) 111-30-8 Carbamates 3-lodopropynylbutylcarbamate (IPBC) 55406-53-6 1-(3-Chloroallyl)-3,5,7-triaza-1- 4080-31 -3 azoniaadamantane chloride (CTAC) Formaldehyde 1,3-Dimethylol-5,5-dimethylhydantoin 6440-58-0 Releasing (DMDMH) Compounds 4,4-dimethyloxazolidine (DMO) 51200-87-4 1,2-Benzisothiazolin-3-one (BIT) 2634-33-5 HeterocyclicN, Mixture of 26172-55-4 S Compounds 5-chloro-2-methyl-4-isothiazolin-3-one and 2-methyl-4-isothiazolin-3-one (CMIT/MIT) 2-Methyl-4-isothiazolin-3-one (MIT) 2682-20-4 2-n-Octyl-4-isothiazolin-3-one (OIT) 26530-20-1 Hydroxymethyl 2-Bromo-2-nitropropane-1,3-diol 52-51-7 Nitroalkanes (Bronopol, BNPD) Classification Microbial pH range Min.
His dissertation focused on the development of new catalytic methods for the preparation of chiral amines and nitroalkanes using diphosphine monoxide ligands.
In these patents it is noted that nitroalkanes as petrol additives reduce nitrogen oxides emissions.
Cueto and Pryor (5) recorded a similar phenomenon and reported that the yellow compound had Fourier-transform infrared spectroscopy (FT-IR)-based assignments from alkyl nitrates, nitroalkanes, and primary nitrocompounds.