216208
Hydrazine dihydrochloride
≥98%
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
NH2NH2 · 2HCl
CAS 번호:
Molecular Weight:
104.97
EC Number:
MDL number:
UNSPSC 코드:
12352300
PubChem Substance ID:
NACRES:
NA.21
Quality Level
분석
≥98%
양식
powder, crystals or chunks
solid
mp
200 °C (dec.) (lit.)
density
1.42 g/mL at 25 °C (lit.)
SMILES string
Cl[H].Cl[H].NN
InChI
1S/2ClH.H4N2/c;;1-2/h2*1H;1-2H2
InChI key
LIAWOTKNAVAKCX-UHFFFAOYSA-N
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관련 카테고리
일반 설명
Hydrazine dihydrochloride can be used as a reducing agent in the conversion of carbonyls to methylene compounds and α, β-epoxyketones to allylic alcohols. It can also reduce alkenes, alkynes, and nitro groups. In addition, it is used to synthesize hydrazides and dinitrogen-containing heterocycles.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Skin Sens. 1
Storage Class Code
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
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Rapid synthesis of 2, 5-disubstituted 1, 3, 4-oxadiazoles under microwave irradiation.
Bentiss F, et al.
Synthetic Communications, 31(6), 935-938 (2001)
A silver colloid produced by reduction with hydrazine as support for highly sensitive surface-enhanced Raman spectroscopy
Nickel U, et al.
Langmuir, 16(23), 9087-9091 (2000)
Spectrophotometric method for determination of hydrazine.
Watt GW and Chrisp JD.
Analytical Chemistry, 24(12), 2006-2008 (1952)
Accelerated synthesis of 3, 5-disubstituted 4-amino-1, 2, 4-triazoles under microwave irradiation.
Bentiss F, et al.
Tetrahedron Letters, 41(10), 1539-1541 (2000)
Ranendu Sekhar Das et al.
Dalton transactions (Cambridge, England : 2003), 42(11), 4068-4080 (2013-01-24)
PVP capped platinum nano particles (PNP) of 5 nm diameter were prepared and characterized as homogeneous and of spherical nature. At physiological pH range (6.0-8.0), these PNP catalyze the deoxygenation of phenoxazine group containing resazurin (1) by hydrazine. The observed
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