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MilliporeSigma

C88602

Cyanoacetohydrazide

98%

Synonym(s):

Cyanoacetic hydrazide

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25 G

$141.00

$141.00

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About This Item

Linear Formula:
NCCH2CONHNH2
CAS Number:
140-87-4
Molecular Weight:
99.09
NACRES:
NA.22
PubChem Substance ID:
24893112
UNSPSC Code:
12352100
EC Number:
205-437-2
MDL number:
MFCD00007611

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Product Name

Cyanoacetohydrazide, 98%

InChI key

HPHBOJANXDKUQD-UHFFFAOYSA-N

InChI

1S/C3H5N3O/c4-2-1-3(7)6-5/h1,5H2,(H,6,7)

SMILES string

NNC(=O)CC#N

assay

98%

form

powder

mp

108-110 °C (lit.)

Quality Level

100

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1 of 4

This Item
671460B13071B91005
Cyanoacetohydrazide 98%

Sigma-Aldrich

C88602

Cyanoacetohydrazide

Propanoic acid hydrazide ≥90% (GC)

Sigma-Aldrich

671460

Propanoic acid hydrazide

Benzhydrazide 98%

Sigma-Aldrich

B13071

Benzhydrazide

tert-Butyl carbazate 98%

Sigma-Aldrich

B91005

tert-Butyl carbazate

assay

98%

assay

≥90% (GC)

assay

98%

assay

98%

Quality Level

100

Quality Level

100

Quality Level

-

Quality Level

200

form

powder

form

-

form

powder

form

crystals

mp

108-110 °C (lit.)

mp

-

mp

112-114 °C (lit.)

mp

39-42 °C (lit.)

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB4832
STBF9014V
STBC2756V
S62026V
S62026

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X M He et al.
Acta crystallographica. Section A, Foundations of crystallography, 49 ( Pt 1), 10-22 (1993-01-01)
For molecular crystals, a procedure is proposed for interpreting experimentally determined atomic mean square anisotropic displacement parameters (ADPs) in terms of the overall molecular vibration together with internal vibrations with the assumption that the molecule consists of a set of
S H Doss et al.
Archives of pharmacal research, 24(5), 377-384 (2001-11-06)
The reaction of either Digitoxin or Digoxin with cyanoacetic acid hydrazide gave the hydrazone derivatives 3a and 3b respectively. The reactivity of the latter products towards chemical reagents was studied to give heterocyclic derivatives with potential biological activities.
Soad A M El-Hawash et al.
Archiv der Pharmazie, 339(1), 14-23 (2006-01-18)
Two new acetylpyridinehydrazones derived from cyanoacetic acid hydrazide have been synthesized namely: cyanoacetic acid (1-pyridin-3 or 4-yl-ethylidene) hydrazides (1a,b). and some derived ring systems: 2-imino or 2-oxo-2H-chromenes (2a,b and 3a,b), substituted 2-thioxo-2,3-dihydrothiazoles (4a-d), substituted 2-thioxo-2,3-dihydro-6H-thiazolo[4,5-d]pyrimidin-7-ones (5a-d), substituted dihydrothiazoles (7a,b), and

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