hydroquinone diacetate

1,4-benzenediol, 1,4-diacetate

CAS: 1205-91-0 C10 H10 O4 MW: 194.18650000

Identification

Namehydroquinone diacetate
IUPAC(4-acetyloxyphenyl) acetate
CAS Number1205-91-0
EINECS214-887-9
FDA UNII18I4277Z6G
Molecular FormulaC10 H10 O4
Molecular Weight194.18650000
MDL NumberMFCD00011643
Nikkaji NumberJ7.454C
XlogP31.30 (est)

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 123.50 °C. @ 760.00 mm Hg
Boiling Point 282.40 °C. @ 760.00 mm Hg (est)
Flash Point 281.00 °F. TCC ( 138.60 °C. ) (est)
logP (o/w) 0.980 (est)
Soluble in water, 1192 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryinformation only not used for fragrances or flavors
Recommendation for hydroquinone diacetate usage levels up tonot for fragrance use.
Recommendation for hydroquinone diacetate flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

(4- acetyloxyphenyl) acetate 1,4- benzenediol, 1,4-diacetate 1,4- diacetoxybenzene p- diacetoxybenzene PubMed: Highly luminescent and triboluminescent coordination polymers assembled from lanthanide β-diketonates and aromatic bidentate O-donor ligands. PubMed: Molecular recognition and self-assembly special feature: Encapsulated-guest rotation in a self-assembled heterocapsule directed toward a supramolecular gyroscope. PubMed: Synthesis of carbobicyclic compounds via palladium-catalyzed cyclization/hydrosilylation: evidence for reversible silylpalladation. PubMed: Metabolism of coenzyme Q10: biliary and urinary excretion study in guinea pigs. PubMed: Single dose parenteral hyposensitization to poison ivy urushiol in guinea pigs.