| Identification | More | [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 Properties | Back 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 | [biological source]
synthetic | [Odor Type]
animal | [JECFA Number]
705 | [Merck ]
2585 | [Major Application]
flavors and fragrances | [Cosmetics Ingredients Functions]
PERFUMING | [InChI]
1S/C15H14O2/c1-12-7-9-14(10-8-12)17-15(16)11-13-5-3-2-4-6-13/h2-10H,11H2,1H3 | [InChIKey]
OJEQSSJFSNLMLB-UHFFFAOYSA-N | [SMILES]
Cc1ccc(OC(=O)Cc2ccccc2)cc1 | [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 Data | Back Directory | [WGK Germany ]
2
| [RTECS ]
CY1679750
| [TSCA ]
TSCA listed | [HS Code ]
2916.39.7700 | [Storage Class]
11 - Combustible Solids | [Toxicity]
LD50 (g/kg): >5 orally in rats; >5 dermally in rabbits (Food Cosmet. Toxicol.) |
| Hazard Information | Back 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. |
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