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1,2-Diacetylhydrazine / 25 G

Purity: 98 %
Synonym: Diacetylahydrazine; Diacetylhydrazine; Diacetyl hydrazine; N,N'-Diacetylhydrazine; N'-Acetylacetohydrazide; N'-acetyl-acetic acid hydrazide
Molecular Formula: CH3CONHNHCOCH3
Molecular Weight: 116.12
SKU: MND-84253
CAS Number: 3148-73-0
MDL number: MFCD00008673
EC Number: 221-576-1
Form: powder
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 25 G  
138.60 EUR



Safety Information


Hazard Statements

H315
H319
H335
H302 + H312 + H332

Precautionary Statements

P280
P264
P270
P301 + P312
P501
P305 + P351 + P338
P261
P271
P304 + P340 + P312
P405
P302 + P352
P302 + P352 + P312
P362 + P364
P403 + P233
P304 + P340
P330
P321
P264 + P265
P319
P332 + P317
P337 + P317
P301 + P317
P317

Pictograms



Properties

Signal WordWarning
Flash Point (C)Not available
Flash Point (F)Not available
Boiling Point209 °C/15 mmHg (lit.)
Melting Point138-140 °C (lit.)

 Product Description

1,2-Diacetylhydrazine is a chemical compound used as an intermediate in organic synthesis. It is a solid substance known for its role in producing various pharmaceuticals and agrochemicals.

 

Application:

1,2-Diacetylhydrazine is primarily used in the synthesis of pharmaceutical compounds and agrochemicals, acting as an intermediate in the production process.

 

 

Articles:

- Vapor Pressures of Molecular Crystals. XIV. Sulfamide and Diacetylhydrazine

Publication Date: 12 April 2006

Sadao Takagi, Ryuichi Shintani, Hideaki Chihara, Syûzô Seki

https://doi.org/10.1246/bcsj.32.137

 

- Determination of isoniazid, acetylisoniazid, acetylhydrazine and diacetylhydrazine in biological fluids by high-performance liquid chromatography

Publication Date: Available online 29 March 2002

W. Von Sassen, M. Castro-Parra, E. Musch, M. Eichelbaum

https://doi.org/10.1016/0378-4347(85)80075-X

 

- The determination of isoniazid and its metabolites acetylisoniazid, monoacetylhydrazine, diacetylhydrazine, isonicotinic acid and isonicotinylglycine in serum and urine

Publication Date: FEBRUARY 01 1972

G. A. Ellard; P. T. Gammon; S M Wallace

https://doi.org/10.1042/bj1260449