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N-nitropropan-1-amine, also known as 1-nitropropan-2-amine or 2-amino-1-nitropropane, is an organic compound with the chemical formula C3H8N2O2. It is a colorless liquid with a pungent odor and is soluble in water. N-nitropropan-1-amine is primarily used as an intermediate in the synthesis of various chemicals, including pharmaceuticals, dyes, and pesticides. Due to its reactivity and potential to form nitrosoamines, which are known carcinogens, N-nitropropan-1-amine is considered hazardous and requires careful handling and storage. It is also important to note that exposure to this chemical can pose health risks, including irritation to the eyes, skin, and respiratory system, as well as potential long-term effects such as mutations and cancer.

627-07-6

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627-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 627-07-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 627-07:
(5*6)+(4*2)+(3*7)+(2*0)+(1*7)=66
66 % 10 = 6
So 627-07-6 is a valid CAS Registry Number.

627-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Propylnitramine

1.2 Other means of identification

Product number -
Other names 1-Propanamine, N-nitro-

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:627-07-6 SDS

627-07-6Relevant academic research and scientific papers

Safe and Convenient Synthesis of Primary N -Nitramines in the Freon Media

Zharkov, Mikhail N.,Kuchurov, Ilya V.,Fomenkov, Igor V.,Tartakovsky, Vladimir A.,Fedyanin, Ivan V.,Zlotin, Sergei G.

supporting information, p. 1103 - 1108 (2017/02/24)

A convenient one-pot synthesis of primary aliphatic N-nitramines, which includes the nitration of available N,N′-dialkyloxalamides or N-alkylcarbamates with dinitrogen pentoxide in the 1,1,1,2-tetrafluoroethane media followed by ammonolysis of intermediate N-nitroamides in the same solvent has been developed. The method is environmentally safe, and affords target N-nitramines in up to 94% overall yield.

A Novel Synthesis of β-Aminoalkylnitroamines. rac-β-Nitroaminoalanine and N-Nitroethylenediamine, Two Repoted Metabolites from Agaricus silvaticus

Nilsson, Liselott,Noori, Ghazi,Bergman, Rolf,Kesler, Ewa,Sterner, Olov,Wickberg, Boerje

, p. 929 - 934 (2007/10/02)

N-Nitroethylenediamine and rac-β-nitroaminoalanine have been prepared in good yields by the same general method, involving addition of methyl N-nitrocarbamate to aziridine or ethyl aziridine-2-carboxylate, respectively.Additive 13C NMR shift parameters for the nitroamino group have been estimated.

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