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N,N-Dimethylhydrazine

ALDRICH/D161608 - 98%

Synonym: 1,1-Dimethylhydrazine; asym-Dimethylhydrazine

CAS Number: 57-14-7
Empirical Formula (Hill Notation): C2H8N2
Molecular Weight: 60.10
EC Number: 200-316-0
MDL Number: MFCD00007628
Linear Formula: (CH3)2NNH2
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-D161608-5G 5 g
$48.20
1/EA
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45-D161608-500G 500 g
$371.00
1/EA
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FT-NMR Spectra for 1,1-Dimethylhydrazine.
FT-IR Spectra for 1,1-Dimethylhydrazine.

 

assay 98%
autoignition temp. 478 °F
bp 60-62 °C (lit.)
density 0.79 g/mL at 20 °C (lit.)
expl. lim. 95 %
form liquid
InChI 1S/C2H8N2/c1-4(2)3/h3H2,1-2H3
InChI key RHUYHJGZWVXEHW-UHFFFAOYSA-N
refractive index n20/D 1.4075 (lit.)
SMILES string CN(C)N
storage temp. 2-8°C
vapor density 1.94 (vs air)
vapor pressure 103 mmHg ( 20 °C)
Application: N,N-Dimethylhydrazine can react with:
• β-Naphthol via radical amination to form 1-amino-2-naphthol.
• 2-Chloro- and 2,2-dichloro-(bromo)vinyl ketones via regioselective heterocyclization to form 3-substituted 1-methyl(5-halo)pyrazoles.
• Terminal alkynes in the presence of TpRuCl(PPh3)2 (Tp = tris(pyrazolyl)borate) to form nitriles.


N,N-Dimethylhydrazine along with ferric chloride hexahydrate forms an effective reduction system for:
• Synthesizing DNA binding pyrrolo[2,1-c][1,4]benzodiazepine (PBD) imines via reductive cyclization of the corresponding nitro aldehyde.
• Transforming a variety of nitroarenes and azido compounds into the corresponding anilines and amino compounds, respectively.

Biochem/physiol Actions: Lung and colon tumor initiator in experimental animal model.
Packaging: 5, 100, 500 g in glass bottle
Purity 98%
bp 60-62 °C (lit.)
Density 0.79 g/mL at 20 °C (lit.)
Refractive Index n20/D 1.4075 (lit.)
Storage Temp. 2-8°C
UNSPSC 12352100

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