Skip to Content
Merck
All Photos(2)

Documents

C11006

Sigma-Aldrich

Carbohydrazide

98%

Synonym(s):

1,3-Diaminourea, Carbodihydrazide, Carbonohydrazide, N,N′-Diaminourea

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
CO(NHNH2)2
CAS Number:
497-18-7
Molecular Weight:
90.08
Beilstein:
1747069
EC Number:
207-837-2
MDL number:
MFCD00007591
UNSPSC Code:
12352100
PubChem Substance ID:
24892343
NACRES:
NA.22

Assay

98%

form

crystals

mp

150-153 °C (lit.)

SMILES string

NNC(=O)NN

InChI

1S/CH6N4O/c2-4-1(6)5-3/h2-3H2,(H2,4,5,6)

InChI key

XEVRDFDBXJMZFG-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Carbohydrazide can be used:
  • As an oxygen scavenger.
  • In the synthesis of polydentate Schiff base ligands with various aldehydes and ligands by condensation.
  • In the synthesis of trifluoromethyl-containing (E)-N′-arylidene-1H-pyrazole-1-carbohydrazides by cyclocondensation reaction which shows antioxidant and antimicrobial properties.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H315,H317,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1

Supplementary Hazards

EUH044

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Marta Kisiel et al.
Journal of controlled release : official journal of the Controlled Release Society, 162(3), 646-653 (2012-08-21)
Understanding the influence of formulation and storage conditions on rhBMP-2 bioactivity is extremely important for its clinical application. Reports in the literature show that different research groups employ different parameters such as formulation conditions, storage, doses for in vivo applications
Ameen Ali Abu-Hashem et al.
Acta pharmaceutica (Zagreb, Croatia), 60(3), 311-323 (2010-12-08)
2-Amino-5-acetyl-4-methyl-thiophene-3-carboxylic acid ethyl ester (1) and 5-acetyl-2-amino-4-methylthiophene-3-carbohydrazide (2) were synthesized and used as starting materials for the synthesis of new series of 1-(5-amino-4-(3,5-dimethyl-1H-pyrazole-1-carbonyl)-3-methylthiophen-2-yl) ethanone (3a), 1-(5-amino-4-(4-chloro-3,5-dimethyl-1H-pyrazole-1-carbonyl)-3-methylthiophen-2-yl) ethanone (3b), 1-(4-methyl-2-amino-5-acetylthiophene-3-carbonyl)pyrazolidine-3,5-dione (4), (Z)-N'-(4-methyl-2-amino-5-acetylthiophene-3-carbonyl) formohydrazonic acid (5a), (Z)-ethyl-N'-4-methyl-2-amino-5-acetylthiophene-3-carbonylformo hydrazonate (5b), 6-acetyl-3-amino-2,5-dimethylthieno[2,3-d]pyrimidin-4(3H)-one (8), 5-methyl-3-amino-2-mercapto-6-acetylthieno
Mateusz Wierzbicki et al.
Nanoscale research letters, 14(1), 320-320 (2019-10-12)
Antibacterial surfaces coated with nanomaterials, including silver nanoparticles, are considered effective alternative antimicrobial agents that can be used instead of antibiotics and chemical agents. However, reports of the potential toxicity of these materials raise questions about the safety of their
Synthesis, structure and reactivity of zirconium (IV), vanadium (IV), cobalt (II), nickel (II) and copper (II) complexes derived from carbohydrazide schiff base ligands.
Warad, DU, et al.
Indian Journal of Chemistry, 39A(10), 415-420 (2000)
Isabelle Tomassoli et al.
European journal of medicinal chemistry, 46(1), 1-10 (2010-11-30)
The synthesis, biological evaluation, and molecular modeling of new 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxamides(4), 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carbohydrazide (6), and some hexahydropyrimido[5,4-c]quinoline-2,5-diones (9) produced earlier by our laboratory, as AChE/BuChE inhibitors, is described. From these analyses compound 4c resulted equipotent regarding the inhibition of cholinesterases'; inhibitors 6k
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service