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Suberic acid(CAS#505-48-6)

Chemical Property:

Molecular Formula C8H14O4
Molar Mass 174.19
Density 1.3010 (rough estimate)
Melting Point 140-144°C(lit.)
Boling Point 230°C15mm Hg(lit.)
Flash Point 203 °C
Water Solubility 0.6 g/L (20 ºC)
Solubility Soluble in water (1.6 mg/ml at 20 °C), DMSO, methanol, and ether (very slightly). Inso
Vapor Presure 0Pa at 22.85℃
Appearance White-like crystal
Color White to cream
Merck 14,8862
BRN 1210161
pKa 4.52(at 25℃)
PH 3.79(1 mM solution);3.27(10 mM solution);2.76(100 mM solution);
Storage Condition Store below +30°C.
Stability Stable. Combustible. Incompatible with strong oxidizing agents, reducing agents, bases.
Refractive Index 1.4370 (estimate)
MDL MFCD00004428
Physical and Chemical Properties Melting point 140-144°C(lit.)

boiling point 230 ° C 15mm Hg(lit.)

flash point 203°C
water solubility 0.6g/L (20°C)
Merck 14,8862
BRN 1210161

Use It mainly reacts with diols and diamine to produce polyester and polyamide. Used for the preparation of special high temperature resistant polymers. It is also used in organic synthesis. It is also used as a pharmaceutical intermediate.

Product Detail

Product Tags

Hazard Symbols Xi – Irritant
Risk Codes R36 – Irritating to the eyes
R36/37/38 – Irritating to eyes, respiratory system and skin.
Safety Description S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S39 – Wear eye / face protection.
S36 – Wear suitable protective clothing.
WGK Germany 1
TSCA Yes
HS Code 29171990

 

Introduction

Caprylic acid is a colorless crystalline solid. It is stable in nature, insoluble in water but soluble in organic solvents. Caprylic acid has a characteristic sour taste.

 

Caprylic acid has a wide range of uses in industry. It is mainly used in the preparation of polyester resin, which is used in the manufacture of coatings, plastics, rubber, fibers and polyester films, etc.

 

There are many ways to prepare octanoic acid. One of the common methods is to prepare it by oxidation of octene. The specific step is to oxidize octene to caprylyl glycol, and then the caprylyl glycol is dehydrated to produce caprylic acid.

Caprylic acid is irritating to the skin and eyes, so it needs to be washed promptly after contact. Appropriate protective equipment should be worn during operation to avoid inhaling its vapors. Caprylic acid should be stored in a dry, well-ventilated place, away from heat and fire.


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