ChemicalBook > CAS DataBase List > FEMA 2860

FEMA 2860

Product Name: FEMA 2860
CAS No.: 94-47-3
Chemical Name: FEMA 2860
Synonyms: FEMA 2860;202-284-3;Phenethylbenzoat;PHENETHYL BENZOATE;PHENYLETHYLBENZOAT;FEMA 2860 USP/EP/BP;PHENYLETHYL BENZOATE;2-Phenethyl benzoate;2-phenylethylbenzoate;2-Phenylethyl benzoate
CBNumber: CB1283363
Molecular Formula: C15H14O2
Formula Weight: 226.27
MOL File: 94-47-3.mol

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FEMA 2860 Property

Boiling point:: 182 °C12 mm Hg(lit.)
Density: 1.093 g/mL at 25 °C(lit.)
vapor pressure: 0.015Pa at 25℃
refractive index: n20/D 1.56(lit.)
FEMA: 2860 | PHENETHYL BENZOATE
Flash point:: >230 °F
solubility: Insoluble in water, soluble in alcohol and oils.
form: Liquid
color: Clear colorless
Odor: at 100.00 %. soft rose balsam honey floral
Odor Type: floral
biological source: synthetic
Water Solubility: 207.21mg/L at 25℃
LogP: 3.815 at 25℃
CAS DataBase Reference: 94-47-3
EPA Substance Registry System: Benzoic acid, 2-phenylethyl ester (94-47-3)

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Safety

WGK Germany: 2
RTECS: DH6288000
HS Code: 29163100
Toxicity: The acute oral LD₅₀ in rats was reported to be 5 g/kg and the acute dermal LD₅₀ in rabbits exceeded 5 g/kg (Wohl 1974).

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P273Avoid release to the environment.

P391Collect spillage. Hazardous to the aquatic environment

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: W286001
Product name: Phenethyl benzoate
Purity: ≥99%, FG
Packaging: sample-k
Price: $53.8
Updated: 2022/05/15

TCI Chemical

Product number: P2893
Product name: Phenethyl Benzoate
Purity: min. 98.0 %
Packaging: 25G
Price: $38
Updated: 2025/07/31

TCI Chemical

Product number: P2893
Product name: Phenethyl Benzoate
Purity: min. 98.0 %
Packaging: 500G
Price: $224
Updated: 2025/07/31

TRC

Product number: P296015
Product name: Phenethyl benzoate
Packaging: 250g
Price: $145
Updated: 2021/12/16

AK Scientific

Product number: J55813
Product name: Phenethyl benzoate
Packaging: 1g
Price: $10
Updated: 2021/12/16

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FEMA 2860 Chemical Properties,Usage,Production

Chemical Properties

Clear colorless liquid

Chemical Properties

Phenethyl benzoate has a sweet, rose and honey-like odor. It is used in trace quantities for fixation of honey, strawberry and other fruit preserves.

Occurrence

Reported found in the essential oil from flowers of rose and orange, in bilberry, cinnamon leaf, cassia leaf, malay apple and sea buckthorn.

Uses

Phenethyl Benzoate is a building block used in the synthetic preparation of esters using Bi(OTf)3 catalyzed acylation of alcohols with acid anhydrides.

Definition

ChEBI: Phenethyl benzoate is a benzoate ester resulting from the formal condensation of the carboxy group of benzoic acid with the hydroxy group of 2-phenylethanol. It has a role as a plant metabolite and a volatile oil component. It is functionally related to a benzoic acid and a 2-phenylethanol.

Application

Phenylethyl Benzoate is used in Carnation, Neroli, Rose and Oriental bases mostly as a fixative and a blender/modifier in the heavier portion of the fragrance. It is a good base for Peony and other delicate florals and blends well with most of the conventional “middle notes”. This material is also used in flavour compositions in minute traces for fixation of Honey, Strawberry and various fruit types. The concentration is normally as low as 1 to 4 ppm in the finished product.

Preparation

From phenethyl alcohol and benzoyl chloride in the presence of NaOH; from phenylethyl alcohol and methylbenzoate; by esterification of phenylethyl acohol with benzoic acid.

Flammability and Explosibility

Not classified

Metabolism

The metabolism of benzoic acid has been extensively studied in more than 20 species, including man (Williams, 1959). Depending on species and other factors, such as availability of glycine, benzoic acid may be excreted in the urine as hippuric acid, benzoyl glucuronide or other compounds (see, for example, Bridges. French. Smith & Williams, 1970; Irjala, 1972; Kato, 1972; Martin, 1966; Runyan, 1971; Strahl & Barr, 1971; Wan & Riegelman, 1972). The major route of biotransformation of benzoic acid in man is conjugation with glycine to form hippuric acid, the rate-limiting factor in this reaction being the availability of glycine (Amsel & Levy. 1969). In man at a dose of 1 mg/kg, benzoic acid is excreted entirely as hippuric acid (Bridges et al. 1970). Phenylethyl alcohol is oxidized almost entirely to phenylacetic acid (Williams, 1959). In rabbits, a small amount of benzoic acid is also formed; the phenylacetic acid is excreted mainly as phenaceturic acid (Smith, Smithies & Williams, 1954).

FEMA 2860 Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from FEMA 2860 manufacturers

Shandong Juchuang Chemical Co., LTD

Product: Phenylethyl Benzoate 94-47-3
Price: US $15.00-13.00/kg
Min. Order: 500kg
Purity: 99.9
Supply Ability: 200ton
Release date: 2024-03-14

Career Henan Chemical Co

Product: FEMA 2860 94-47-3
Price: US $3.00/KG
Min. Order: 1KG
Purity: 99%
Supply Ability: 100kg
Release date: 2019-09-03

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2-Phenylethyl benzoate

2-phenylethylbenzoate

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benzylcarbinylbenzoate

beta-Phenethyl benzoate

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phenethylalcohol,benzoate

B-PHENYLETHYL BENZOATE

BENZOIC ACID PHENETHYL ESTER

BETA PHENYL ETHYL BENZOATE

FEMA 2860

PHENETHYL BENZOATE, 98+%

Benzoic acid phenethyl

PHENETHYL BENZOATE 99+%

2-Phenethyl benzoate

Phenethylbenzoat

PHENYLETHYLBENZOAT

FEMA 2860 USP/EP/BP

202-284-3

TIANFU CHEM 94-47-3 FEMA 2860

94-47-3

C6H5COOC2H4C6H5

C6H5CO2CH2CH2C6H5

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