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Propionaldehyde dimethyl hydrazone, also known as 3-dimethylaminopropylamine or 3-dimethylamino-1-propylamine, is an organic compound with the chemical formula C5H13N. It is a colorless liquid that is soluble in water and has a strong, fishy odor. Propionaldehyde dimethyl hydrazone is formed by the reaction of propionaldehyde with dimethyl hydrazine, and it is used as a reagent in various chemical analyses, particularly in the detection of aldehydes and ketones. It is also employed as a building block in the synthesis of pharmaceuticals and other organic compounds. Due to its potential health risks, including irritation to the eyes, skin, and respiratory system, as well as its classification as a hazardous substance, it is important to handle propionaldehyde dimethyl hydrazone with care and in accordance with safety regulations.

7422-93-7

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7422-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7422-93-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,2 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7422-93:
(6*7)+(5*4)+(4*2)+(3*2)+(2*9)+(1*3)=97
97 % 10 = 7
So 7422-93-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2/c1-4-5-6-7(2)3/h5H,4H2,1-3H3

7422-93-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-N-[(E)-propylideneamino]methanamine

1.2 Other means of identification

Product number -
Other names Propanal,dimethylhydrazone

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:7422-93-7 SDS

7422-93-7Relevant academic research and scientific papers

Catalytic hydrophosphorylation of alkyl- and acylhydrazones

Matveeva,Podrugina,Kolesnikova,Prisyazhnoi,Karateev,Zefirov

experimental part, p. 418 - 424 (2011/02/17)

N-Boc- and N-acylhydrazino phosphonates were obtained for the first time by hydrophos- phorylation of the appropriate hydrazones of aliphatic and aromatic aldehydes and heterocyclic and aliphatic ketones in the presence of [tetra(tert-butyl)phthalocyanine

A short access to 3-hydroxy-4-hydroxymethyltetrahydrofurans: Application to the total synthesis of amphiasterin B4

Salim, Hani,Piva, Olivier

supporting information; experimental part, p. 2257 - 2260 (2009/08/07)

The first total synthesis of amphiasterin B4, a secondary metabolite previously isolated from Plakortis quasiamphiaster has been achieved. The core structure has been reached according to a highly stereoselective one-pot epoxidation/cyclization of an unsa

A novel, one-pot synthesis of α-C-cyanohydrazines in the presence of lithium perchlorate/diethylether solution (5.0 M)

Heydari, Akbar,Baharfar, Robabe,Rezaie, Mohsen,Aslanzadeh, Saied M.

, p. 368 - 369 (2007/10/03)

Condensation of N,N-dimethylhydrazine, an aldehyde in lithium perchlorate/diethylether solution (5.0 M) gave N,N-dimethylhydrazone, which were treated with trimethylsilylcyanide to afford α-C-cyanohydrazine. These compounds are important precursors of nitrogen-substituted reagents.

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