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Merck
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Documentos

12309

Supelco

p-Benzoquinona

for spectrophotometric det. of amines, ≥99.5% (HPLC)

Sinônimo(s):

Quinona

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About This Item

Fórmula linear:
C6H4(=O)2
Número CAS:
Peso molecular:
108.09
Beilstein:
773967
Número CE:
Número MDL:
Código UNSPSC:
12352005
ID de substância PubChem:
NACRES:
NA.21

densidade de vapor

3.73 (vs air)

Nível de qualidade

pressão de vapor

0.1 mmHg ( 25 °C)

Ensaio

≥99.5% (HPLC)

forma

powder or crystals

temperatura de autoignição

815 °F

qualidade

for spectrophotometric det. of amines

técnica(s)

UV/Vis spectroscopy: suitable

resíduo de sublimação

≤0.1%

cor

, Faint Yellow to Very Dark Yellow to Very Dark Beige and Green-Yellow

pf

112-114 °C
113-115 °C (lit.)

cadeia de caracteres SMILES

O=C1C=CC(=O)C=C1

InChI

1S/C6H4O2/c7-5-1-2-6(8)4-3-5/h1-4H

chave InChI

AZQWKYJCGOJGHM-UHFFFAOYSA-N

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Aplicação

P-Benzoquinone along with tetrathiafulvalene (TTF) was used as mediators, in an experimental study based on different parameters affecting the preparation of enzyme electrochemical biosensors using self-assembled monolayer (SAM)-modified electrodes is reported. It may be used for spectrophotometric determination of cysteine and/or carbocysteine in a mixture of amino acids, shampoo, and pharmaceutical. It may also be used as an effective cogent in peroxide-initiated crosslinking of polypropylene.

Outras notas

Reagent for the spectrophotometric microdetermination of amines

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Flam. Sol. 1 - Muta. 2 - Skin Corr. 1B - Skin Sens. 1 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

4.1B - Flammable solid hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

170.6 °F - closed cup

Ponto de fulgor (°C)

77 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Spectrophotometric microdetermination of amines and sulfamates with 1,4-Benzoquinone.
G A Benson et al.
Analytical chemistry, 48(14), 2149-2152 (1976-12-01)
Preparation, characterization and application of alkanethiol self-assembled monolayers modified with tetrathiafulvalene and glucose oxidase at a gold disk electrode.
Campuzano S
Journal of Electroanalytical Chemistry, 526 (1), 92-100 (2002)
Peroxide-initiated crosslinking of polypropylene in the presence of p-benzoquinone.
Chodak I and Lazar M.
Journal of Polymer Science: Part A, General Papers, 32 (6), 5432-5437 (1986)
D A Zaia et al.
Talanta, 50(5), 1003-1010 (2008-10-31)
A simple, sensitive, and selective method has been developed for determination of cysteine (Cys) or carbocysteine (carboCys) in pharmaceutical products, shampoos and a mixture of amino acids. The results showed the reaction between p-benzoquinone (PBQ) and Cys occurs through the
Vandana Bhalla et al.
Dalton transactions (Cambridge, England : 2003), 42(4), 975-980 (2012-11-21)
A pentaquinone based compound 3a has been synthesized which undergoes significant fluorescence enhancement in the presence of Zn(2+) ions with a detection limit up to nanomolar range in THF. Further, the zinc ensemble of 3a is evaluated for its anti-oxidizing

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