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Ethyl crotonate(CAS#623-70-1)

Chemical Property:

Molecular Formula C6H10O2
Molar Mass 114.14
Density 0.918g/mLat 25°C(lit.)
Melting Point 37.22°C (estimate)
Boling Point 142-143°C(lit.)
Flash Point 36°F
JECFA Number 1806
Water Solubility INSOLUBLE
Vapor Presure 65 hPa (50 °C)
Vapor Density 3.9 (vs air)
Appearance Liquid
Color Clear colorless
Merck 14,2597
BRN 635834
Storage Condition Store below +30°C.
Stability Stable. Highly flammable. Incompatible with strong oxidizing agents.
Refractive Index n20/D 1.424(lit.)
Physical and Chemical Properties Colorless to light yellow liquid. Boiling point 136 degrees C, flash point 22 degrees Celsius. It has a strong acid-burning aroma and fruit aroma, with a flavor of rum and ether. Natural products are found in apples, papaya, strawberries, rum, wine, and cocoa.

Product Detail

Product Tags

Risk Codes R11 – Highly Flammable
R34 – Causes burns
R36 – Irritating to the eyes
Safety Description S16 – 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.
S45 – In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S9 – Keep container in a well-ventilated place.
S33 – Take precautionary measures against static discharges.
UN IDs UN 1862 3/PG 2
WGK Germany 2
RTECS GQ3500000
TSCA Yes
HS Code 29161980
Hazard Class 3
Packing Group II
Toxicity LD50 orally in Rabbit: 3000 mg/kg

 

Introduction

Ethyl trans-butenoate is an organic compound. The following is an introduction to the properties, uses, preparation methods and safety information of the compound:

 

Quality:

Ethyl trans-butenoate is a colorless liquid with a peculiar odor. It is slightly denser than water with a density of 0.9 g/mL. Soluble in a variety of organic solvents, such as ethanol, ethers and naphthenes, at room temperature.

 

Use:

Ethyl trans-butenate has a variety of applications in the chemical industry. The most common use is as an intermediate in organic synthesis for the preparation of other organic compounds, such as oxalates, ester solvents and polymers. It can also be used as coatings, rubber adjuvants, and solvents.

 

Method:

The preparation method of trans-butenoate ethyl ester is generally obtained by the reaction of trans-butenoic acid with ethanol. This product is obtained by heating trans-butenic acid and ethanol under acidic conditions to form an ester.

 

Safety Information:

Ethyl trans-butenoate is irritating to the eyes and skin and may cause inflammation of the eyes and skin. Inhalation of its vapours should be avoided when handling the compound, and operations should be carried out in a well-ventilated area. When storing, it should be placed in an airtight container, away from ignition and oxidizers.

 


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