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5-Octanolide(CAS#698-76-0)

Chemical Property:

Molecular Formula C8H14O2
Molar Mass 142.2
Density 1,002 g/cm3
Melting Point -14°C
Boling Point 238°C
Flash Point 125°C
JECFA Number 228
Water Solubility Not miscible or difficult to mix in water.
Solubility Chloroform (Slightly), Methanol (Slightly)
Vapor Presure 1.5-2.7Pa at 20-25℃
Appearance neat
Specific Gravity 1.00
Color Colourless
BRN 111515
Storage Condition Sealed in dry,Room Temperature
Stability Hygroscopic
Refractive Index 1.4550
Physical and Chemical Properties Colorless to light yellow liquid, cocoa, coconut and milk fat like aroma.

Product Detail

Product Tags

Risk Codes R36/37/38 – Irritating to eyes, respiratory system and skin.
R36/38 – Irritating to eyes and skin.
Safety Description S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 – Wear suitable protective clothing.
S37 – Wear suitable gloves.
WGK Germany 2
RTECS UQ1355500
TSCA Yes
HS Code 29322090
Toxicity LD50 orl-rat: >5 g/kg FCTOD7 20,783,80

 

Introduction

δ-Octanolactone, also known as caprolactone, is an organic compound. It is a colorless to pale yellow liquid with a characteristic aroma of octanol. The following is an introduction to the properties, uses, preparation methods and safety information of δ-octanololide:

 

Quality:

- δ-Octanolactone is a volatile liquid that is soluble in water and many organic solvents.

- It is an unstable compound that is susceptible to polymerization and hydrolysis.

- It has low viscosity, low surface tension and good wetability.

 

Use:

- δ-Octanolactone is used in a wide range of applications, including plastics manufacturing, polymer synthesis, and surface coatings.

- It can be used as a component of solvents, catalysts and plasticizers.

- In the field of polymers, δ-octanol lactone can be used to prepare polycaprolactone (PCL) and other polymers.

- It can also be used in medical devices, coatings, adhesives, encapsulation materials, etc.

 

Method:

- δ-Octololide can be prepared by esterification of ε-caprolactone.

- The reaction is usually carried out under appropriate reaction conditions by reacting ε-caprolactone with an acid catalyst such as methanesulfonic acid.

- The preparation process requires control of reaction temperature and time to obtain a high-purity product.

 

Safety Information:

- It can be irritating to the skin, eyes, and respiratory tract and should be avoided when touched.

- During use and storage, it is necessary to maintain a well-ventilated environment and avoid fire sources and high temperatures.

- When disposing of waste, it should be handled and disposed of in accordance with local regulations.


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