1,2-Diethylhydrazine dihydrochloride

Base Information

• Chemical Name: 1,2-Diethylhydrazine dihydrochloride
• CAS No.: 7699-31-2
• Molecular Formula: C₄H₁₂N₂*2ClH
• Molecular Weight: 161.075
• Hs Code.: 2928000090
• European Community (EC) Number: 624-628-5
• UN Number: 2811
• UNII: X3O3IWE4TG
• DSSTox Substance ID: DTXSID2025056
• Wikidata: Q27293520
• ChEMBL ID: CHEMBL1203769
• Mol file: 7699-31-2.mol

Synonyms:1,2-Diethylhydrazine dihydrochloride;7699-31-2;N,N'-Diethylhydrazine dihydrochloride;1,2-diethylhydrazine;dihydrochloride;CCRIS 8919;Hydrazine, 1,2-diethyl-, dihydrochloride;UNII-X3O3IWE4TG;X3O3IWE4TG;1,2-Diethylhydrazine 2HCl;N',N'-Diethylhydrazine Dihydrochloride;diethylhydrazine dihydrochloride;SCHEMBL3118416;CHEMBL1203769;DTXSID2025056;NMTDWUVFGOBBAX-UHFFFAOYSA-N;MFCD00012523;1,2-diethyl hydrazine dihydrochloride;1,2-diethylhydrazine dihydrochlo-ride;AKOS015913271;LS-1707;AS-81659;CS-0343044;FT-0606394;Hydrazine,1,2-diethyl-,hydrochloride(1:2);Q27293520;HYDRAZINE, 1,2-DIETHYL-, HYDROCHLORIDE (1:2)

Chemical Property of 1,2-Diethylhydrazine dihydrochloride

Chemical Property:

• Melting Point: 169 °C (dec.)(lit.)
• Boiling Point: 84.7 °C at 760 mmHg
• PSA: 24.06000
• LogP: 2.50620
• Storage Temp.: Room Temperature
• Solubility.: DMSO, Methanol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 160.0534038
• Heavy Atom Count: 8
• Complexity: 17.5
• Transport DOT Label: Poison

Purity/Quality:

99%, ^*data from raw suppliers

N’,N’-DiethylhydrazineDihydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 45-20/21/22-36/37/38
• Safety Statements: 53-26-36/37/39-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Nitrogen Compounds -> Hydrazines
• Canonical SMILES: CCNNCC.Cl.Cl
• Uses: Reactant involved in:? ;Bromopyridazinedione-mediated protein and peptide bioconjugation1? ;Synthesis of human neutrophil proteinase 3 inhibitors2? ;Three-component cascade processes for sythesis of aminoisoindolones and phthalazones3? ;Stereoselective heterocyclization for synthesis of substituted hexahydropyrazolodiazepinecarboxylates4? ;Synthesis of azacycloalkanes, isoindoles, pyrazole, pyrazolidine, and phthalazine derivatives5 Reactant involved in:Bromopyridazinedione-mediated protein and peptide bioconjugationSynthesis of human neutrophil proteinase 3 inhibitorsThree-component cascade processes for sythesis of aminoisoindolones and phthalazonesStereoselective heterocyclization for synthesis of substituted hexahydropyrazolodiazepinecarboxylatesSynthesis of azacycloalkanes, isoindoles, pyrazole, pyrazolidine, and phthalazine derivatives