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Merck

225819

Sigma-Aldrich

Hydrazin Hydrat

reagent grade, N2H4 50-60 %

Synonym(e):

Hydraziniumhydroxid

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About This Item

Lineare Formel:
NH2NH2 · xH2O
CAS-Nummer:
Molekulargewicht:
32.05 (anhydrous basis)
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352302
PubChem Substanz-ID:
NACRES:
NA.21

Qualität

reagent grade

Qualitätsniveau

Dampfdichte

>1 (vs air)

Dampfdruck

5 mmHg ( 25 °C)

Form

liquid

Zusammensetzung

Degree of hydration, ~1.5
N2H4, 50-60%

Expl.-Gr.

99.99 %

Konzentration

50.0-60.0% (%H4N2 by Na2S2O3 basis, titration)

Dichte

1.029 g/mL at 25 °C (lit.)

SMILES String

NN.[H]O[H]

InChI

1S/H4N2.H2O/c1-2;/h1-2H2;1H2

InChIKey

IKDUDTNKRLTJSI-UHFFFAOYSA-N

Verwandte Kategorien

Allgemeine Beschreibung

The addition of hydrazine hydrate to reduced graphene oxide (RGO) counter electrode improves its performance in dye-sensitized solar cells (DSSC).

Anwendung

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.

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Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - Skin Sens. 1

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

204.8 °F - closed cup

Flammpunkt (°C)

96 °C - closed cup

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Kunden haben sich ebenfalls angesehen

T Baumann et al.
Scientific reports, 5, 15194-15194 (2015-10-16)
Enamel proteins form a scaffold for growing hydroxyapatite crystals during enamel formation. They are then almost completely degraded during enamel maturation, resulting in a protein content of only 1% (w/v) in mature enamel. Nevertheless, this small amount of remaining proteins
Reduction of aromatic nitro compounds with hydrazine hydrate in the presence of an iron oxide hydroxide catalyst. I. The reduction of monosubstituted nitrobenzenes with hydrazine hydrate in the presence of ferrihydrite.
Lauwiner M, et al.
Applied Catalysis A: General, 172(1), 141-148 (1998)
Graphite catalyzed reduction of aromatic and aliphatic nitro compounds with hydrazine hydrate.
Byung HH, et al.
Tetrahedron Letters, 26(50), 6233-6234 (1985)
Catalytic reduction of nitroarenes with hydrazine hydrate in suitable solvents.
Ayyangar NR, et al.
Synthesis, 1981(08), 640-643 (1981)
Synthesis and molecular structure of 3-(2-benzyloxy-6-hydroxyphenyl)-5-styrylpyrazoles. Reaction of 2-styrylchromones and hydrazine hydrate.
Pinto DC, et al.
Tetrahedron, 55(33), 10187-10200 (1999)

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