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83353

Sigma-Aldrich

Mercury(II) bromide

puriss. p.a., ACS reagent, ≥99.0% (precipitation titration)

Sinônimo(s):

Mercuric bromide

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About This Item

Fórmula linear:
HgBr2
Número CAS:
Peso molecular:
360.40
Número CE:
Número MDL:
Código UNSPSC:
12352302
ID de substância PubChem:
NACRES:
NB.24
Ensaio:
≥99.0% (precipitation titration)
Formulário:
powder or crystals

grau

ACS reagent
puriss. p.a.

Nível de qualidade

pressão de vapor

1 mmHg ( 136.5 °C)

Ensaio

≥99.0% (precipitation titration)

Formulário

powder or crystals

resíduo de ignição (após redução)

≤0.02%

p.e.

322 °C (lit.)

pf

236 °C (lit.)

traços de ânion

chloride (Cl-): ≤2000 mg/kg
sulfate (SO42-): ≤50 mg/kg

traços de cátion

Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

cadeia de caracteres SMILES

Br[Hg]Br

InChI

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

chave InChI

NGYIMTKLQULBOO-UHFFFAOYSA-L

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Descrição geral

Mercury(II) bromide (HgBr2) affords 1:1 adducts on reaction with N,N,N′,N′- tetramethyl-o-phenylenediamine (o-Me2N.C6H4.NMe2). Single-crystal X-ray diffraction studies of these adducts have been reported.

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 1 Dermal - Acute Tox. 1 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Código de classe de armazenamento

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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Crystal Structures of the 1: 1 Adducts of N, N, N', N'-Tetramethyl-o-phenylenediamine with Zinc (II) Bromide and Mercury (II) Bromide and Iodide.
Hughes CM, et al.
Australian Journal of Chemistry, 38(10), 1521-1527 (1985)
M E Goodsite et al.
Environmental science & technology, 38(6), 1772-1776 (2004-04-13)
The oxidation of elemental mercury (Hg0) to the divalent gaseous mercury dibromide (HgBr2) has been proposed to account for the removal of Hg0 during depletion events in the springtime Arctic. The mechanism of this process is explored in this paper
G Medgyes et al.
Carbohydrate research, 186(2), 225-239 (1989-03-15)
D-Galactose was converted into the glycosylating agents 4-azido-2,3-di-O-benzyl-4-deoxy-6-O-propionyl-alpha-D-glucopyranosyl chloride (11) and the methyl beta-D-thiopyranoside 19. Condensation of 11 with 2,5-diazido-1,6-di-O-benzoyl-2,5-di-deoxy-L-iditol in the presence of mercury salts gave 24% of 2,5-diazido-3-O-(4-azido-2,3-di-O-benzyl-4-deoxy-6-O-propionyl-alp ha-D- glucopyranosyl)-1,6-di-O-benzoyl-2,5-dideoxy-L-iditol. Methyl trifluoromethanesulfonate-promoted glycosylation of 1,3-diazido-2-O-benzyl-1,3-dideoxy-5,6-O-isopropylidene-D-gulit ol with 19
Olivier Gueldry et al.
European journal of biochemistry, 270(11), 2486-2496 (2003-05-21)
In Saccharomyces cerevisiae, disruption of the YCF1 gene increases the sensitivity of cell growth to mercury. Transformation of the resulting ycf1 null mutant with a plasmid harbouring YCF1 under the control of the GAL promoter largely restores the wild-type resistance
S Engst et al.
Biochemistry, 37(33), 11496-11507 (1998-08-26)
Conditions are described under which the nonphysiological substrate mercuric bromide (HgBr2) is rapidly turned over, both by the wild type (CCCC) and by an active site double mutant (CCAA) of mercuric reductase in which the C-terminal cysteines 557' and 558'

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