Skip to Content
Merck
CN
All Photos(1)

Documents

229172

Sigma-Aldrich

1,2-Diethylhydrazine dihydrochloride

Sign Into View Organizational & Contract Pricing

Linear Formula:
C2H5NHNHC2H5 · 2HCl
CAS Number:
Molecular Weight:
161.07
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

mp

169 °C (dec.) (lit.)

SMILES string

Cl[H].Cl[H].CCNNCC

InChI

1S/C4H12N2.2ClH/c1-3-5-6-4-2;;/h5-6H,3-4H2,1-2H3;2*1H

InChI key

NMTDWUVFGOBBAX-UHFFFAOYSA-N

Related Categories

Application

1,2-Diethylhydrazine dihydrochloride was used in the synthesis of 4,5-dihydro-pyrazole, pyrazolidine and 1,2-dihydro-phthalazine derivatives.
Reactant involved in:
  • Bromopyridazinedione-mediated protein and peptide bioconjugation
  • Synthesis of human neutrophil proteinase 3 inhibitors
  • Three-component cascade processes for sythesis of aminoisoindolones and phthalazones
  • Stereoselective heterocyclization for synthesis of substituted hexahydropyrazolodiazepinecarboxylates
  • Synthesis of azacycloalkanes, isoindoles, pyrazole, pyrazolidine, and phthalazine derivatives

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Yuhong Ju et al.
The Journal of organic chemistry, 71(1), 135-141 (2006-01-04)
[reactions: see text] The synthesis of nitrogen-containing heterocycles from alkyl dihalides (ditosylates) and primary amines and hydrazines via a simple and efficient cyclocondensation in an alkaline aqueous medium that occurs under microwave irradiation is described. This improved greener synthetic methodology

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service