7119-92-8 Usage
Description
N-nitrodiethylamine is a highly toxic and potentially carcinogenic chemical compound, characterized by its yellow, oily liquid appearance and distinct odor. It is highly volatile and poses significant health and environmental risks.
Uses
Used in Dye Production:
N-nitrodiethylamine is used as an intermediate in the production of various dyes, contributing to the synthesis of colorants for different applications.
Used in Pharmaceutical Industry:
N-nitrodiethylamine serves as a key component in the manufacturing process of certain pharmaceuticals, playing a crucial role in the development of specific medications.
Used in Pesticide Production:
This chemical compound is also utilized in the production of pesticides, where it acts as an essential ingredient for creating effective and targeted crop protection solutions.
Due to the hazardous nature of N-nitrodiethylamine, its use is strictly regulated and limited in many countries. It is imperative to follow proper handling and disposal procedures to mitigate the associated environmental and health risks, including liver and lung damage, as well as an increased risk of certain types of cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 7119-92-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,1 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7119-92:
(6*7)+(5*1)+(4*1)+(3*9)+(2*9)+(1*2)=98
98 % 10 = 8
So 7119-92-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H10N2O2/c1-3-5(4-2)6(7)8/h3-4H2,1-2H3
7119-92-8Relevant articles and documents
Synthesis of N,N-dialkylnitramines from secondary ammonium nitrates in liquid or supercritical carbon dioxide
Kuchurov,Fomenkov,Zlotin
experimental part, p. 2058 - 2062 (2011/01/08)
An efficient explosion-proof method was developed for the preparation of N,N-dialkylnitramines by treatment of dialkylammonium nitrates with a mixture of nitric acid and acetic anhydride in the presence of ZnCl2 in liduid or supercritical carbon dioxide.
ANODIC NITRATION OF SECONDARY AMINES
Evtyugin, G. A.,Gol'frid, V. U.,Semanov, D. A.,Latypova, V. Z.,Kargin, Yu. M.,et al.
, p. 2497 - 2498 (2007/10/02)
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N-Nitration of amides. VII. Kinetics of the nitrolysis of N,N-dialkylamides of carboxylic acids by nitronium tetrafluoroborate in acetonitrile
Andreev, S. A.,Lebedev, B. A.,Tselinskii, I. V.
, p. 1166 - 1170 (2007/10/02)
The kinetics of the nitrolysis of amides R2NC(O)R', where R=C2H5, R'=tert-C4H9, iso-C4H9, C4H9, iso-C3H7, C3H7, CH3, CH2Cl, CH2CN, CCl3; R'=CH3, R=CH3, C3H7, C4H9, by nitronium tetrafluoroborate in an acetonitrile medium were investigated.It was established that the polar effect of the substituents in the acyl group of the amides (R') shows up mostly in the overallrate of the process.The effect of substituents at the nitrogen atom (R) is due to the steric effects of the alkyl groups.
