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About This Item
Empirical Formula (Hill Notation):
C2H8N2 · C2H2O4
CAS Number:
Molecular Weight:
150.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3697941
Assay:
≥96.0% (T)
Quality Level
assay
≥96.0% (T)
impurities
~2% hydrazine
mp
170-173 °C (dec.)
functional group
amine, carboxylic acid, hydrazine
SMILES string
CCNN.OC(=O)C(O)=O
InChI
1S/C2H8N2.C2H2O4/c1-2-4-3;3-1(4)2(5)6/h4H,2-3H2,1H3;(H,3,4)(H,5,6)
InChI key
DUMHBFMURBWDPC-UHFFFAOYSA-N
Application
Ethylhydrazine oxalate can be used to synthesize:
- 1-ethyl-1H-indazoles
- 3-substituted 1-ethyl-6-methylpyrimido[4,5-c]pyridazine-5,7(1H,6H)-dione derivatives
- 4-(2-alkyl-5-methyl-2H-pyrazol-3-yl)-piperidines
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 1B - Skin Sens. 1
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
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Find documentation for the products that you have recently purchased in the Document Library.
Regioselective synthesis of 4-(2-alkyl-5-methyl-2H-pyrazol-3-yl)-piperidines.
Dirat O, et al.
Tetrahedron Letters, 47(11), 1729-1731 (2016)
Parallel Synthesis of Novel 3-Substituted 1-Ethyl-6-methylpyrimido [4, 5-c] pyridazine-5, 7 (1 H, 6 H)-dione Analogs.
Chen Y, et al.
Synthetic Communications, 40(6), 821-832 (2010)
A method for the regioselective synthesis of 1-alkyl-1H-indazoles.
Liu HJ, et al.
Tetrahedron, 69(19), 3907-3912 (2013)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| D171301-25G | 04061831826463 |
| 04100-25G | 04061838629043 |
| 04100-5G | 04061832097558 |


