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Methyl phenylacetate

CAS No.
101-41-7
Chemical Name:
Methyl phenylacetate
Synonyms
Methyl 2-phenylacetate;Methylphenylacetat;PHENYLACETIC ACID METHYL ESTER;2-phenylpropanoate;Methyl benzeneacetate;FEMA 2733;Mephaneine;METHYL A-TOLUATE;METHYLPAROXETINE;METHYL-PHENYLACETAT
CBNumber:
CB1333473
Molecular Formula:
C9H10O2
Molecular Weight:
150.17
MDL Number:
MFCD00008453
MOL File:
101-41-7.mol
MSDS File:
SDS
Last updated:2024-04-16 18:29:06

Methyl phenylacetate 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
Odor at 10.00 % in dipropylene glycol. sweet floral honey spice waxy almond
Odor Type honey
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℃
Substances Added to Food (formerly EAFUS) METHYL PHENYLACETATE
FDA 21 CFR 172.515
CAS DataBase Reference 101-41-7(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII D4PDC41X96
NIST Chemistry Reference Benzeneacetic acid, methyl ester(101-41-7)
EPA Substance Registry System Methyl phenylacetate (101-41-7)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
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
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).
NFPA 704
2
0 0

Methyl phenylacetate price More Price(26)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W273309 Methyl phenylacetate ≥98%, FCC, FG 101-41-7 1kg $79.8 2024-03-01 Buy
Sigma-Aldrich W273309 Methyl phenylacetate ≥98%, FCC, FG 101-41-7 10Kg $461 2024-03-01 Buy
Sigma-Aldrich 108057 Methyl phenylacetate ReagentPlus , ≥99% 101-41-7 100g $41.6 2024-03-01 Buy
Sigma-Aldrich W273309 Methyl phenylacetate ≥98%, FCC, FG 101-41-7 5kg $305 2023-06-20 Buy
Sigma-Aldrich 42958 Methyl phenylacetate analytical standard 101-41-7 1ml $62.8 2022-05-15 Buy
Product number Packaging Price Buy
W273309 1kg $79.8 Buy
W273309 10Kg $461 Buy
108057 100g $41.6 Buy
W273309 5kg $305 Buy
42958 1ml $62.8 Buy

Methyl phenylacetate Chemical Properties,Uses,Production

Chemical Properties

Methyl phenylacetate is a clear colorless liquid that is only slightly soluble in water, but very soluble in most organic solvents. It has a strong odor similar to honey. The odor is so strong that recommended smelling is of a solution with 10% or less methyl phenyl acetate. This compound also naturally occurs in brandy, capsicum, coffee, honey, pepper and some wine.

Occurrence

Reported found in cocoa, coffee, strawberry, pineapple, pepper, hop oil, cognac, peanut, honey, starfruit, Bourbon vanilla, mountain papaya, roasted chicory root and rooibus tea (Aspalathus linearis).

Uses

Methyl phenylacetate is utilized for partition coefficient measurement experiments. It is mainly used in the flavor industry and in perfumes to impart honey scents. Further, it acts as a precursor to prepare synthetic perfumes. It acts as an acylating agent and involved in the enantioselective acylation of beta-lactam intermediate using penicillin G amidase.

Application

Methyl Phenylacetate is used as a reagent in the synthesis of various organic reactions, one of which is the synthesis of Vulpinic Acid; a lichen metabolite with anti-inflammatory properties. It is also used in the formulation of edible flavors, for the preparation of honey, chocolate, tobacco and other flavors; it can also be used in daily chemical flavors for the preparation of rose, oriental flavors and other flavors. IFRA has no restrictions.

Preparation

Methyl phenylacetate is synthesized from phenylacetonitrile by hydrolysis and esterification. Put methanol into a dry glass-lined reaction pot, stir and cool to below 30°C, add sulfuric acid dropwise, heat up to 90°C after adding, and start adding phenylacetonitrile dropwise, control the temperature at about 95°C, and finish adding in 1.5h. After reacting at 95-100 °C for 6 h, it was cooled to below 40 °C and diluted with water equivalent to about 0.6 times the reaction solution. The acid water was separated by standing, and a saturated sodium carbonate solution was added for neutralization and washing, and the aqueous layer was discarded. It is dehydrated with anhydrous calcium chloride and fractionated under reduced pressure to obtain methyl phenylacetate with a yield of 80%.

Definition

ChEBI: Methyl benzeneacetate is a member of benzenes. It is a flavoring ingredient. Odoriferous constituent of many plants. It is generally found in brandy, capsicum, honey, pepper, some wine, coca and coca products.

Aroma threshold values

Detection: 25 ppb

Taste threshold values

Taste characteristics at 30 ppm: floral, fruity, honey, spice, waxy and sweet

Synthesis Reference(s)

Journal of the American Chemical Society, 93, p. 4919, 1971 DOI: 10.1021/ja00748a051
Tetrahedron Letters, 30, p. 2945, 1989 DOI: 10.1016/S0040-4039(00)99165-2

General Description

Methyl phenylacetate has been identified in the volatile fraction of beewax absolute oil, dried fruiting bodies of Boletus auripes, Chinese fermented black soybeans and peated malt.

Biochem/physiol Actions

Methyl phenylacetate undergoes decomposition on photolysis in methanol. Methyl phenylacetate acts as acylating agent and causes the enantioselective acylation of beta-lactam intermediate using penicillin G amidase. Methyl phenylacetate is the starting material in manufacture of synthetic perfumes.

Safety Profile

Moderately toxic by ingestion and skin contact. A skin irritant. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS.

616-38-6
103-79-7
101-41-7
Synthesis of Methyl phenylacetate from Dimethyl carbonate and Phenylacetone
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View Lastest Price from Methyl phenylacetate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Methyl phenylacetate pictures 2024-04-25 Methyl phenylacetate
101-41-7
US $10.00 / G 1G 99% 20 CONTIDE BIOTECH CO.,LTD
 Methyl Phenylacetate pictures 2024-04-25 Methyl Phenylacetate
101-41-7
US $10.00-5.00 / kg 1kg 99.5 10 ton per month Nanjing Deda New Material Technology Co., Ltd
Methyl phenylacetate pictures 2024-04-19 Methyl phenylacetate
101-41-7
US $6.80 / kg 1kg 99% 5MT ZHEJIANG JIUZHOU CHEM CO., LTD
Acetic acid, phenyl-, methyl ester METHYL ALPHA-TOLUATE METHYL BENZYLFORMATE METHYL A-TOLUATE METHYL PHENYLACETATE FEMA 2733 Methyl phenylacetate/Phenylacetic acid methyl ester Phenylacetic Acid Phenylacetate METHYL PHENYLACETATE 98+% FCC METHYL PHENYLACETATE, 99+% Methyl phenylacetate (technical) Phenylacetic acid, methyl ester (technical) METHYL-PHENYLACETAT METHYLPAROXETINE Methyl phenylacetate >=99.0% Methyl phenylacetate, 99+% 250ML Methyl phenylacetate Vetec(TM) reagent grade, 98% 2-Phenylacetic acid methyl Phenylacetic acid methyl Methyl phenylacetate ReagentPlus(R), >=99% Benzeneaceticacid,methylester Mephaneine Methyl ester of Phenylacetic acid methyl phenylethanoate methylalpha-phenylacetate methylbenzeneacetate methylbenzeneethanoate methylphenylethanoate phenyl-aceticacimethylester MethylPhenylacetate> Methyl DL-mandelate Powder Methyl phenylacetate USP/EP/BP Methyl phenylacetate(kosher) Hotselling CAS?101-41-7?Methyl Phenylacetate Methylphenylacetat PHENYLACETIC ACID METHYL ESTER Methyl 2-phenylacetate Methyl benzeneacetate 2-phenylpropanoate Ipratropium Bromide Impurity 24 Lenacapavir (GS-6207) 101-41-7 C6H5CH2CO2CH3 C6H5CH2COOCH3 C8 to C9 Carbonyl Compounds Building Blocks Organic Building Blocks Esters Pharmaceutical Intermediates flavoring Organics C8 to C9 Carbonyl Compounds Esters API intermediates Alphabetical Listings Flavors and Fragrances