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Merck
모든 사진(2)

주요 문서

200085

Sigma-Aldrich

Mercury(II) bromide

ACS reagent

동의어(들):

Mercuric bromide

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100 G
₩412,598

₩412,598


예상 입고일2025년 4월 14일세부사항


벌크 견적 요청

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100 G
₩412,598

About This Item

Linear Formula:
HgBr2
CAS Number:
Molecular Weight:
360.40
EC Number:
MDL number:
UNSPSC 코드:
12352302
PubChem Substance ID:
NACRES:
NB.24

₩412,598


예상 입고일2025년 4월 14일세부사항


벌크 견적 요청

Grade

ACS reagent

vapor pressure

1 mmHg ( 136.5 °C)

양식

powder

반응 적합성

reagent type: catalyst
core: mercury

불순물

≤0.05% insol. CH3OH

산화 잔류물

≤0.02%

색상

white to very faintly yellow

bp

322 °C (lit.)

mp

236 °C (lit.)

음이온 미량물

chloride (Cl-): ≤0.25%

SMILES string

Br[Hg]Br

InChI

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

InChI key

NGYIMTKLQULBOO-UHFFFAOYSA-L

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일반 설명

Mercury(II) bromide (HgBr2) affords 1:1 adducts on reaction with N,N,N′,N′- tetramethyl-o-phenylenediamine. Single-crystal X-ray diffraction studies of these adducts have been reported.[1] It forms complexes by reacting with 3,12-dimethylbenzo[a]quinoxalino[2,3-c]phenazine ligand.[2]

애플리케이션

Mercury(II) bromide (HgBr2) may be used in the preparation of mononuclear [Hg(L1)Br2] and 1D polymer [Hg2(L2)Br4]n [L1 = (N,N-diethyl,N′-(pyridin-2-yl)formylidene)ethane-1,2-diamine and L2 = (N,N-diethyl,N′-(pyridin-2-yl)benzylidene)ethane-1,2-diamine].[3] It may also be used as a promoter in the glycoslyation reaction of alcohols.[4]

픽토그램

Skull and crossbonesHealth hazardEnvironment

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

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

Storage Class Code

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


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문서 라이브러리 방문

이미 열람한 고객

Synthesis of Quinoxalinophenazine Derivatives and Reaction of 3, 12-Dimethylbenzo [a] quinoxalino [2, 3-c] phenazine with Mercury (II) Bromide: Spectral and Structural Characterization.
Marjani AP, et al.
Chinese Journal of Structural Chemistry / Jie Gou Hua Xue, 33(10), 1460-1466 (2014)
Syntheses, Structures and Properties of Two Luminous Mercury (II) Bromides Containing Tridentate N-Donor Schiff Bases: Control of Coordination Number and Nuclearity by Varying Ligand Matrices.
Satapathi S, et al.
Journal of Chemical Crystallography, 42(10), 1060-1066 (2012)
Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-?-d-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters.
Carvalho I, et al.
Carbohydrate Research, 338(10), 1039-1043 (2003)
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)
Don S Forsyth et al.
Food additives and contaminants, 21(9), 849-856 (2005-01-26)
Mercury was detected in all analysed samples of swordfish, marlin, shark and tuna purchased from major supermarket outlets and fish retailers in three cities across Canada. Total mercury and methylmercury levels ranged up to 3845 and 2346 ng g(-1), respectively.

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