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Merck
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Key Documents

13-1930

Sigma-Aldrich

Hydroquinone

JIS special grade, ≥99.0%

Sinônimo(s):

1,4-Benzenediol, 1,4-Dihydroxybenzene, HQ

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About This Item

Fórmula linear:
C6H4-1,4-(OH)2
Número CAS:
Peso molecular:
110.11
Beilstein:
605970
Número CE:
Número MDL:
Código UNSPSC:
12352002
ID de substância PubChem:

grau

JIS special grade

densidade de vapor

3.81 (vs air)

pressão de vapor

1 mmHg ( 132 °C)

Ensaio

≥99.0%

forma

crystalline

temperatura de autoignição

930 °F

disponibilidade

available only in Japan

pH

3.7 (70 g/L)

pb

285 °C (lit.)

pf

172-175 °C (lit.)

solubilidade

water: soluble 50 g/L

cadeia de caracteres SMILES

Oc1ccc(O)cc1

InChI

1S/C6H6O2/c7-5-1-2-6(8)4-3-5/h1-4,7-8H

chave InChI

QIGBRXMKCJKVMJ-UHFFFAOYSA-N

Procurando produtos similares? Visita Guia de comparação de produtos

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Muta. 2 - Skin Sens. 1B

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

329.0 °F - closed cup

Ponto de fulgor (°C)

165 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


Certificados de análise (COA)

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Visite a Biblioteca de Documentos

P Carbonnelle et al.
Toxicology and applied pharmacology, 132(2), 220-226 (1995-06-01)
Decreased interleukin-1 (IL-1) production by mononuclear phagocytes has been shown to contribute to benzene myelotoxicity in animals. The study presented here was designed to examine the relevance of this mechanism in humans. Fresh human blood monocytes were exposed to 0.001-10
Yaqi Hu et al.
Biosensors & bioelectronics, 47, 45-49 (2013-04-03)
A novel light "on-off" photoelectrochemical sensing for the sensitive determination of hydroquinone was developed based on the porphyrin-functionalized Au nanoparticles on graphene (porphyrin/AuNPs/graphene). Gold nanoparticles (AuNPs) were firstly modified onto graphene sheets using NaBH4 as reductant and the porphyrin/AuNPs/graphene nanocomposites
Jacob Levitt
Journal of the American Academy of Dermatology, 57(5), 854-872 (2007-05-01)
Recently, the US Food and Drug Administration proposed a ban on over-the-counter hydroquinone mainly on the basis of high absorption, reports of exogenous ochronosis in humans, and murine hepatic adenomas, renal adenomas, and leukemia with large doses over extended time
Douglas McGregor
Critical reviews in toxicology, 37(10), 887-914 (2007-11-21)
The toxicology of hydroquinone has been reviewed on a number of previous occasions. This review targets its potential for carcinogenicity and possible modes of carcinogenic action. The evaluation made by IARC (1999) of its carcinogenic risk to humans was that
A P DeCaprio
Critical reviews in toxicology, 29(3), 283-330 (1999-06-24)
Hydroquinone (HQ) is a high-volume commodity chemical used as a reducing agent, antioxidant, polymerization inhibitor, and chemical intermediate. It is also used in over-the-counter (OTC) drugs as an ingredient in skin lighteners and is a natural ingredient in many plant-derived

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