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Merck
CN

215465

氯化汞(II)

ACS reagent, ≥99.5%

别名:

二氯化汞

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线性分子式:
HgCl2
化学文摘社编号:
分子量:
271.50
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-299-8
MDL number:
Assay:
≥99.5%
Grade:
ACS reagent
Form:
powder
Solubility:
acetic acid: soluble(lit.)
acetone: soluble in salt form(lit.)
alcohol: soluble(lit.)
diethyl ether: passes test
ethyl acetate: soluble(lit.)
glycerol: soluble(lit.)
water: soluble(lit.)
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产品名称

氯化汞(II), ACS reagent, ≥99.5%

assay

≥99.5%

form

powder

vapor pressure

1.3 mmHg ( 236 °C)

InChI key

LWJROJCJINYWOX-UHFFFAOYSA-L

InChI

1S/2ClH.Hg/h2*1H;/q;;+2/p-2

SMILES string

Cl[Hg]Cl

grade

ACS reagent

reaction suitability

reagent type: catalyst
core: mercury

reduction residue

≤0.02%

mp

277 °C (lit.)

solubility

acetic acid: soluble(lit.)
acetone: soluble in salt form(lit.)
alcohol: soluble(lit.)
diethyl ether: passes test
ethyl acetate: soluble(lit.)
glycerol: soluble(lit.)
water: soluble(lit.)

cation traces

Fe: ≤0.002%

Quality Level

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Application

Mercury (II) chloride can be used as a catalyst for the:
  • Addition reaction between aromatic amines to terminal acetylenes to give imines, enamines, and 1,2,3,4-tetrahydroquinoline derivatives.
  • Cyclization of amidinothioureas with phenyl hydrazine to produce 3-amino-1,2,4-triazole derivatives.
  • Cyclization of O-propargyl glycolaldehyde dithioacetals to afford 3-pyranones along with 2,5-dihydrofuran-3-carboxaldehydes through their dithioketals and dithioacetals reaction.
  • Reductive dimerization and cyclization of α,β-unsaturated ketones produce functionalized cyclopentanols using N,N-dimethylformamide as solvent.

General description

Mercury (II) chloride is an inorganic salt commonly used as a catalyst in organic synthesis.

signalword

Danger

Hazard Classifications

Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Muta. 2 - Repr. 2 - Skin Corr. 1B - STOT RE 1

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

监管及禁止进口产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Ashley E Peppriell et al.
Toxicology, 443, 152561-152561 (2020-08-18)
Methylmercury (MeHg) is a ubiquitous environmental contaminant and developmental toxicant known to cause a variety of persistent motor and cognitive deficits. While previous research has focused predominantly on neurotoxic MeHg effects, emerging evidence points to a myotoxic role whereby MeHg
Mercury(II) Chloride.
Koc ovsky P.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2001)
Eagleson M.
Concise Encyclopedia Chemistry, 498-498 (1994)
Vasco Branco et al.
Free radical biology & medicine, 52(4), 781-793 (2011-12-27)
Mercury compounds exert toxic effects via interaction with many vital enzymes involved in antioxidant regulation, such as selenoenzymes thioredoxin reductase (TrxR) and glutathione peroxidase (GPx). Selenium supplementation can reactivate the mercury-inhibited TrxR and recover the cell viability in vitro. To
Igor Shuryak et al.
Scientific reports, 9(1), 11361-11361 (2019-08-08)
Exposure to chronic ionizing radiation (CIR) from nuclear power plant accidents, acts of terrorism, and space exploration poses serious threats to humans. Fungi are a group of highly radiation-resistant eukaryotes, and an understanding of fungal CIR resistance mechanisms holds the

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