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ETHYL METHYLPHENYLGLYCIDATE

Ethyl methylphenylglycidate

CAS: 77-83-8

Molecular Formula: C12H14O3

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ETHYL METHYLPHENYLGLYCIDATE - Names and Identifiers

Name Ethyl methylphenylglycidate
Synonyms EMPG
fraesol
Aldehyde c16
bayberry aldehyde
Strawberry aldehyde
Ethylmethylphenyglycidate
Ethylmethylphenylglycidate
Ethyl methylphenylglycidate
Ethyl methyl phenylglycidate
Ethyl 3-methyl-3-phenylglycidate
Ethyl 2,3-epoxy-3-phenyl butanoate
2,3-epoxy-3-phenyl-butanoicaciethylester
2,3-Epoxy-3-phenylbutyric acid, ethyl ester
ethyl 2,3-epoxy-3-methyl-3-phenylpropionate
ethyl 3-methyl-3-phenyloxirane-2-carboxylate
ethyl ester of 2,3-epoxy-3-phenylbutanoic acid
3-methyl-3-phenyl-oxiranecarboxylicaciethylester
ethyl alpha,beta-epoxy-beta-methylhydrocinnamate
3-methyl-3-phenyl-oxiranecarboxylicacidethylester
3-methyl-3-phenyl-oxiranecarboxylicacid,ethylester
3-methyl-3-phenyloxiranecarboxylic acid ethyl ester
ethyl (2R,3S)-3-methyl-3-phenyloxirane-2-carboxylate
ethyl (2S,3R)-3-methyl-3-phenyloxirane-2-carboxylate
ethyl (2S,3S)-3-methyl-3-phenyloxirane-2-carboxylate
ethyl (2R,3R)-3-methyl-3-phenyloxirane-2-carboxylate
alpha,beta-epoxy-beta-methyl-hydrocinnamicaciethylester
alpha,beta-epoxy-beta-methylhydrocinnamicacid,ethylester
Ethyl 3-methyl-3-phenylglycidate, mixture of cis and trans
alpha,beta-Epoxy-beta-methylhydrocinnamic acid, ethyl ester
CAS 77-83-8
EINECS 201-061-8
InChI InChI=1/C12H14O3/c1-3-14-11(13)10-12(2,15-10)9-7-5-4-6-8-9/h4-8,10H,3H2,1-2H3/t10-,12-/m1/s1

ETHYL METHYLPHENYLGLYCIDATE - Physico-chemical Properties

Molecular FormulaC12H14O3
Molar Mass206.24
Density1.087g/mLat 25°C(lit.)
Melting Point33.0 -38.0℃
Boling Point272-275°C(lit.)
Flash Point>230°F
JECFA Number1577
Vapor Presure0.00571mmHg at 25°C
Appearanceclear liquid
ColorColorless to Light orange to Yellow
BRN12299
Storage Condition2-8°C
Refractive Indexn20/D 1.505(lit.)
Physical and Chemical PropertiesColorless to light yellow liquid with strong strawberry fruit aroma. Boiling point 260 °c. Soluble in ethanol, ether, can be miscible with diethyl phthalate, insoluble in water and glycerol. Rat oral LD505.47g/kg,ADI 0~0.5mg/kg(FAO/WHO,1996).

ETHYL METHYLPHENYLGLYCIDATE - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk CodesR10 - Flammable
R36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS16 - Keep away from sources of ignition.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
UN IDsUN 1993 3/PG 3
WGK Germany2
RTECSMW5250000
TSCAYes
HS Code29189090
ToxicityLD50 orally in Rabbit: 5470 mg/kg

ETHYL METHYLPHENYLGLYCIDATE - Nature

Open Data Verified Data

colorless to light yellow liquid with strong strawberry fruit aroma. Boiling point 260 °c. Soluble in ethanol, ether. Miscible with diethyl phthalate, insoluble in water and glycerol.

Last Update:2024-01-02 23:10:35

ETHYL METHYLPHENYLGLYCIDATE - Hair-making

Open Data Verified Data

The acetophenone is condensed with ethyl chloroacetate in the presence of sodium ethoxide or sodium amino acid, neutralized, washed with water, separated, and distilled under reduced pressure.

Last Update:2022-01-01 10:07:40

ETHYL METHYLPHENYLGLYCIDATE - Use

Open Data Verified Data

for the preparation of cherry, grape, apple, strawberry and other fruit-based food flavor. The dosage of gum is 470mg/kg; 5.6mg/kg in soft drink; 21mg/kg in candy; 18mg/kg in baked food; 13mg/kg in pudding; 6.7 mg/kg in cold drinks.

Last Update:2022-01-01 10:07:41

ETHYL METHYLPHENYLGLYCIDATE - Reference Information

FEMA2444 | ETHYL METHYLPHENYLGLYCIDATE
NIST chemical information information provided by: webbook.nist.gov (external link)
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
content analysis method 1 approximately 1g of a sample is weighed precisely and determined by Method 1 in the ester determination method (OT-18). The equivalence factor (e) in the calculation is taken as 103.1. Methods two by gas chromatography (GT-10-4) determination. The conditions were: column 1.6 m x internal diameter glass column. The filler is to improve the past polyethylene glycol 20M(SPl000)4%, the carrier is diatomite carrier. Gas is helium or nitrogen; Flow rate 50ml/min. The detector was used with an FID and the operating temperature was 250 °c. Column temperature: Isothermal section about 200 deg C; Sample temperature of about 225 deg C. A sample of 1.0 μl was taken and injected into the gas chromatograph. The resulting chromatogram had two main peaks that were essentially equal in height, two isomers of cis-and-myricetin, with several shorter peaks around them., The content of chimonaldehyde can be determined from the height or Peak area of the peaks of the cis-and trans-isomers.
toxicity Adl 0-0.5mg/kg(FAO/WHO,1994). GRAS(FDA,182.60,2000)LD50 5470mg/kg (rat, oral).
usage limit FEMA(mg/kg): soft drinks 5.6; Cold drinks 6.7 candy 21; Baked goods 18; pudding 13; Gum 470
Use strawberry aldehyde is a food Spice temporarily allowed to be used in China's "health standards for the use of food additives, mainly used in the preparation of cherry, grape, apple, strawberry and other fruit-based food flavor. The dosage of gum is 470mg/kg; 5.6mg/kg in soft drinks, 21mg/kg in candy; 18mg/kg in baked food; 13mg/kg in pudding; 6.7 mg/kg in cold drinks.
for the deployment of daily chemical flavor and feed flavor
In the Daily flavor, in the edible flavor is often used
GB 2760 a 96 provisions for the temporary use of edible spices. Mainly used in the preparation of strawberry, cherry, apple flavor, and often with the use of fourteen aldehyde.
This product has a strong red bayberry flavor, usually used as a blending raw material of Red Bayberry flavor after dilution, and also used in cosmetics, when blending rose, Hyacinth and cyclamen and other cosmetics, add trace amounts of this product can produce special effects.
production method This product is non-synthetic, which is composed of acetophenone and ethyl chloroacetate condensed in the presence of sodium ethoxide, that is, it was prepared by Claisen reaction. Based on acetophenone, the yield is about 40%.
add fine powder sodium amino acid to benzene (or xylene) mixture of phenylacetone and ethyl chloroacetate with stirring, keep at 15-20 ℃ for 4 hours, add ice, the oil layer was obtained by vacuum distillation after washing.
The product is obtained by condensation of ethyl chloroacetate with acetophenone in the presence of sodium amino acid or sodium ethoxide, neutralization, washing with water and separation after completion of the reaction, followed by atmospheric distillation and then distillation under reduced pressure.
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-06-20 15:49:28
ETHYL METHYLPHENYLGLYCIDATE
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View History
ETHYL METHYLPHENYLGLYCIDATE
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