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D8402

1,2-Diacetylhydrazine

Name: 1,2-Diacetylhydrazine
Brand: ALDRICH

98%

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About This Item

Linear Formula:

CH₃CONHNHCOCH₃

CAS Number:

3148-73-0

Molecular Weight:

116.12

NACRES:

NA.22

PubChem Substance ID:

24894211

UNSPSC Code:

12352100

EC Number:

221-576-1

MDL number:

MFCD00008673

Assay:

98%

Form:

powder

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Properties

Quality Level

100

assay

98%

form

powder

bp

209 °C/15 mmHg (lit.)

mp

138-140 °C (lit.)

SMILES string

CC(=O)NNC(C)=O

InChI

1S/C4H8N2O2/c1-3(7)5-6-4(2)8/h1-2H3,(H,5,7)(H,6,8)

InChI key

ZLHNYIHIHQEHJQ-UHFFFAOYSA-N

Description

pictograms

GHS07

signalword

Warning

hcodes

H302 + H312 + H332,H315,H319,H335

pcodes

P261 - P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Levels of acetyl hydrazines and rate of acetylation of isoniazid in adult tuberculosis patients.

E B Bhalerao et al.

Indian journal of physiology and pharmacology, 29(2), 83-88 (1985-04-01)

Patients suffering from pulmonary tuberculosis were investigated for the levels of isoniazid (INH) and its metabolites viz. acetyl-INH, mono and diacetyl hydrazines and ammonia. It was observed that 50% of the patients are slow inactivators of INH and almost all

Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 2. N-substituted phenoxysulfenate derivatives.

Qiqi Zhao et al.

Journal of agricultural and food chemistry, 56(13), 5254-5259 (2008-06-11)

A series of novel N-substituted phenoxysulfenyl- N'- tert-butyl- N, N'-diacylhydrazines were designed and synthesized as insect growth regulators via the key intermediates N-chlorosulfenyl- N'- tert-butyl- N, N'-diacylhydrazines. Compared to the parent compounds, these N-substituted phenoxysulfenyl derivatives displayed better solubility and

Double N-H bond activation of N,N'-bis-substituted hydrazines with stable N-heterocyclic silylene.

Ramachandran Azhakar et al.

Dalton transactions (Cambridge, England : 2003), 41(5), 1529-1533 (2011-12-14)

The reaction of N-heterocyclic silylene (NHSi) L [L = CH{(C[double bond, length as m-dash]CH(2))(CMe)(2,6-iPr(2)C(6)H(3)N)(2)}Si] with benzoylhydrazine, 1,2-dicarbethoxyhydrazine, 1,2-diacetylhydrazine and 1,2-bis(tert-butoxycarbonyl)hydrazine in 1 : 1 molar ratio resulted in compounds 1-4 with an almost quantitative yield and five coordinate silicon atoms.

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Global Trade Item Number

SKU	GTIN
D8402-25G	04061838354013