Methyl phenylacetate manufacturers and suppliers

Methyl phenylacetate suppliers

Properties

Melting point:: 107-115 °C

Boiling point:: 218 °C (lit.)

Density: 1.066 g/mL at 20 °C (lit.)

vapor pressure: 16.9-75Pa at 20℃

FEMA: 2733 | METHYL PHENYLACETATE

refractive index: n20/D 1.503(lit.)

Flash point:: 195 °F

storage temp.: Store below +30°C.

solubility: Chloroform (Slightly), Methanol (Slightly)

color: Colourless

Specific Gravity: 1.07

Odor: at 10.00 % in dipropylene glycol. sweet floral honey spice waxy almond

Odor Type: honey

biological source: synthetic

Water Solubility: Miscible with water.

Merck: 14,7268

JECFA Number: 1008

BRN: 878795

Stability:: Stable. Combustible. Incompatible with strong oxidizing agents, strong bases.

InChIKey: CRZQGDNQQAALAY-UHFFFAOYSA-N

LogP: 1.91-2.09 at 21.9-25℃

CAS DataBase Reference: 101-41-7(CAS DataBase Reference)

NIST Chemistry Reference: Benzeneacetic acid, methyl ester(101-41-7)

EPA Substance Registry System: Methyl phenylacetate (101-41-7)

Safety Information

Symbol(GHS): GHS07,GHS08

Signal word: Warning

Hazard statements: H227-H303

Precautionary statements: P210e-P280a-P370+P378a-P403+P235-P501a

Hazard Codes: Xn

Risk Statements: 21-R21

Safety Statements: 23-24/25

WGK Germany: 2

RTECS: AJ3175000

TSCA: Yes

HS Code: 29163500

Hazardous Substances Data: 101-41-7(Hazardous Substances Data)

Toxicity: The acute oral LD₅₀ in rats was reported as 2.55 g/kg (1.67-3.43 g/kg) and the acute dermal LD₅₀ in rabbits as 2.4 g/kg (0.15-4.7 g/kg) (Moreno, 1974).

Use

Methyl phenylacetate belongs to an ester compound form between the methanol and phenylacetate. It chemical formula is C6H5CH2COOCH3. It is generally found in brandy, capsicum, honey, pepper, some wine, coca and coca products. It is mainly used as a flavouring agent, and is also supplemented into perfumes to enhance honey scents. It is also applied for the partition coefficient measurement experiments. It can also be used as the precursor for the manufacture of synthetic perfumes. In addition, as an acylating agent, it can participate in the enantioselective acylation reaction of beta-lactam intermediate catalyzed by the penicillin G amidase.

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