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Ethyl 2,3-epoxy-3-phenylpropionate(CAS#121-39-1)

Chemical Property:

Molecular Formula C11H12O3
Molar Mass 192.21
Density 1.102 g/mL at 25 °C (lit.)
Melting Point 17-18 °C
Boling Point 96 °C/0.5 mmHg (lit.)
Flash Point >230°F
JECFA Number 1576
Water Solubility 748.4mg/L at 24℃
Solubility Insoluble in water
Vapor Presure 0.12Pa at 24℃
Appearance Liquid
Color Clear colorless to yellow
Storage Condition 2-8°C
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
Sensitive Moisture Sensitive
Refractive Index n20/D 1.518(lit.)
Physical and Chemical Properties Colorless to yellowish liquid with strong strawberry-like aroma and strawberry sauce-like taste. Boiling point 228 °c. Miscible in ethanol, ether, chloroform and non-volatile oil, a few insoluble in water, insoluble in propylene glycol and glycerol.

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Risk and Safety

Hazard Symbols Xi – Irritant
Risk Codes 36/37/38 – Irritating to eyes, respiratory system and skin.
Safety Description S23 – Do not breathe vapour.
S24/25 – Avoid contact with skin and eyes.
WGK Germany 2
RTECS MB4970000
TSCA Yes
HS Code 29189990
Toxicity The acute oral LD50 value in rats was reported as 2.3 ml/kg (2.0-2.6 ml/ kg) (Shelanski, 1973b). The acute dermal LD50 value in rabbits was reported as > 5 g/kg (Shelanski, 1973a).

 

 

Ethyl 2,3-epoxy-3-phenylpropionate(CAS#121-39-1) introduction

Ethyl 2,3-epoxy-3-phenylpropionate, also known as ethyl phenylepoxydicarboxylate, is an organic compound. The following is information about its properties, uses, manufacturing methods and safety:

Quality:
Appearance: Colorless liquid.
Density: 1.107 g/cm³.
Solubility: Soluble in organic solvents such as ethanol and ether.

Use:
Ethyl 2,3-epoxy-3-phenylpropionate has important uses in the field of chemistry and is mainly used in the following areas:
As a catalyst and intermediate in organic synthesis to synthesize other organic compounds.
It can be used as a photoinitiator and an additive in coatings.

Method:
The preparation method of ethyl 2,3-epoxy-3-phenylpropionate mainly comprises the following steps:
Benzoic acid and ethyl chloroacetate were added to the reaction tungsten sand catalyst to obtain ethyl phenylacetate by esterification.
Then, ethyl phenylacetate is reacted with hydrogen peroxide under temperature control to generate ethyl 2,3-epoxy-3-phenylpropionate.

Safety Information:
Ethyl 2,3-epoxy-3-phenylpropionate is a chemical that should be handled with protective glasses, gloves and protective clothing to avoid contact with the skin.
Avoid inhaling gases or vapours and operate in a well-ventilated area.
Avoid contact with oxidants and strong acids to avoid dangerous reactions.
If inhaled or ingested, seek medical attention immediately.


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