C11006
Carbohydrazide
98%
Synonym(s):
1,3-Diaminourea, Carbodihydrazide, Carbonohydrazide, N,N′-Diaminourea
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About This Item
Linear Formula:
CO(NHNH2)2
CAS Number:
Molecular Weight:
90.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-837-2
Beilstein/REAXYS Number:
1747069
MDL number:
Assay:
98%
Form:
crystals
Quality Level
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
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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1
supp_hazards
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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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
Alessandro K Jordão et al.
Bioorganic & medicinal chemistry, 19(18), 5605-5611 (2011-08-16)
Tuberculosis treatment remains a challenge that requires new antitubercular agents due to the emergence of multidrug-resistant Mycobacterium strains. This paper describes the synthesis, the antitubercular activity and the theoretical analysis of N-substituted-phenylamino-5-methyl-1H-1,2,3-triazole-4-carbohydrazides (8a-b, 8e-f, 8i-j and 8n-o) and new analogues
Global Trade Item Number
| SKU | GTIN |
|---|---|
| C11006-100G | 04061832493077 |
| C11006-25G | 04061833460719 |