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About This Item
Linear Formula:
NH2NH2 · xH2O
CAS Number:
Molecular Weight:
32.05 (anhydrous basis)
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
206-114-9
MDL number:
Grade:
reagent grade
Form:
liquid
grade
reagent grade
Quality Level
vapor density
>1 (vs air)
vapor pressure
5 mmHg ( 25 °C)
form
liquid
composition
Degree of hydration, ~1.5 , N2H4, 50-60%
expl. lim.
99.99 %
concentration
50.0-60.0% (%H4N2 by Na2S2O3 basis, titration)
density
1.029 g/mL at 25 °C (lit.)
SMILES string
NN.[H]O[H]
InChI
1S/H4N2.H2O/c1-2;/h1-2H2;1H2
InChI key
IKDUDTNKRLTJSI-UHFFFAOYSA-N
General description
The addition of hydrazine hydrate to reduced graphene oxide (RGO) counter electrode improves its performance in dye-sensitized solar cells (DSSC).
Application
Hydrazine hydrate has been used for the deproteination of the enamel samples in a study. It may be used as a reducing agent in the following:
- Preparation of silver nanoparticles.
- Transformation of monosubstituted nitrobenzene derivatives to the corresponding anilines.
- Along with graphite for the conversion of nitro compounds (aromatic and aliphatic) to the amino compounds.
Hydrazine hydrate may be used to prepare:
- 3-(2-Benzyloxy-6-hydroxyphenyl)-5-styrylpyrazoles by reacting with 5-benzyloxy-2-styrylchromones.
- 3,5-Diphenyl-2-pyrazoline derivatives by reacting with 1,3-diphenyl-2-propen-1-one.
- 3′-Aryl-1,2,3,4,4′,5′-hexahydrospiro[quinoxalin-2,5′-pyrazol]-3-ones by reacting with 3-arylacylidene-3,4-dihydroquinoxalin-2(1H)-ones.
- It may also be used in the catalytic reduction of nitroarenes to aromatic amines.
signalword
Danger
flash_point_f
204.8 °F - closed cup
flash_point_c
96 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
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Efficient synthesis of 2-(pyrazol-3-yl) benzimidazoles from 3-arylacylidene-3, 4-dihydroquinoxalin-2 (1H)-ones and hydrazine hydrate via a novel rearrangement.
Mamedov VA, et al.
Tetrahedron Letters, 50(37), 5186-5189 (2009)
Chun-Yu Chen et al.
Polymers, 12(9) (2020-09-20)
Electronic textiles (E-textiles) have been an area of intense industrial and academic research for years due to their advanced applications. Thus, the goal of this study was to develop highly conductive silk fibroin electrochromic nanofibers for use in E-textiles. The
Synthesis and antidepressant activities of some 3, 5-diphenyl-2-pyrazolines.
Palaska E, et al.
The Journal of Organic Chemistry, 36(6), 539-543 (2001)



