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ChemicalBook--->CAS DataBase List--->101-94-0

101-94-0

101-94-0 Structure

101-94-0 Structure
IdentificationMore
[Name]

p-Tolyl phenylacetate
[CAS]

101-94-0
[Synonyms]

4-CRESYL PHENYLACETATE
4-METHYLPHENYL PHENYLACETATE
FEMA 3077
P-CRESYL A-TOLUATE
P-CRESYL PHENYLACETATE
PHENYLACETIC ACID P-CRESYL ESTER
PHENYLACETIC ACID P-TOLYL ESTER
P-TOLYL A-TOLUATE
P-TOLYL PHENYLACETATE
4-methylphenylbenzeneacetate
Acetic acid, phenyl-, p-tolyl ester
Benzeneacetic acid, 4-methylphenyl ester
Benzeneaceticacid,4-methylphenylester
p-Cresyl alpha-toluate
phenyl-aceticacip-tolylester
p-tolyl
p-Tolyl alpha-toluate
P-TOLYL PHENYLACETATE 99+%
CresylPhenylAcetate
p-Cresyl-α-toluate
[EINECS(EC#)]

202-990-1
[Molecular Formula]

C15H14O2
[MDL Number]

MFCD00025983
[Molecular Weight]

226.27
[MOL File]

101-94-0.mol
Chemical PropertiesBack Directory
[Melting point ]

74-76 °C(lit.)
[Boiling point ]

148 °C / 1.5mmHg
[density ]

1.108±0.06 g/cm3(Predicted)
[FEMA ]

3077
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[color ]

White to Almost white
[Odor]

at 10.00 % in dipropylene glycol. animal rose honey narcissus lily hyacinth
[Odor Type]

animal
[JECFA Number]

705
[Merck ]

2585
[LogP]

3.79
[CAS DataBase Reference]

101-94-0(CAS DataBase Reference)
[NIST Chemistry Reference]

Benzeneacetic acid, 4-methylphenyl ester(101-94-0)
[EPA Substance Registry System]

101-94-0(EPA Substance)
Safety DataBack Directory
[WGK Germany ]

2
[RTECS ]

CY1679750
[HS Code ]

2916.39.7700
[Toxicity]

LD50 (g/kg): >5 orally in rats; >5 dermally in rabbits (Food Cosmet. Toxicol.)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Thionyl chloride-->Phenylacetic acid-->p-Cresol
Hazard InformationBack Directory
[Chemical Properties]

p-Cresyl Phenylacetate is prepared by esterification of p-cresol with phenylacetic acid. It forms crystals (mp 75–76°C)with a narcissus odor and a honey note. It is used in blossom compositions with a slight animalic note.
[Chemical Properties]

p-Tolyl phenylacetate has a faint but tenacious lily, hyacinth, narcissus odor with a sweet, honey-like flavor.
[Occurrence]

Has apparently not been reported to occur in nature.
[Uses]

p-Tolyl phenylacetate are used as the ingredients of jasmine, narcissus, hyacinth, lily, and jonquille perfume compositions; fixative;fragrance ingredient in soaps and household products.
[Definition]

ChEBI:P-Tolyl phenylacetate is a benzoate ester and a member of phenols.
[Preparation]

From p-cresol and phenylacetic acid by esterification, or by heating phenylacetyl chloride with freshly distilled p-cresol.
Spectrum DetailBack Directory
[Spectrum Detail]

p-Tolyl phenylacetate(101-94-0)MS
p-Tolyl phenylacetate(101-94-0)1HNMR
p-Tolyl phenylacetate(101-94-0)13CNMR
p-Tolyl phenylacetate(101-94-0)IR1
p-Tolyl phenylacetate(101-94-0)IR2
p-Tolyl phenylacetate(101-94-0)Raman
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

101-94-0(sigmaaldrich)
[TCI AMERICA]

p-Tolyl Phenylacetate,>99.0%(GC)(101-94-0)
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