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Capryl Glycol, 1,2-Octanediol, 1,2-DIHYDROXYOCTANE, 1117-86-8

Capryl Glycol, 1,2-Octanediol, 1,2-DIHYDROXYOCTANE, 1117-86-8

1,2-Octanediol

CAS: 1117-86-8

Molecular Formula: C8H18O2

Names and Identifiers

Name 1,2-Octanediol
Synonyms 1,2-OCTANEDIOL
1,2-Octanediol
Octan-1,2-diol
Octane-1,2-diol
octane-1,2-diol
R,S-Octane-1,2-diol
1,2-Dihydroxyoctane
1,2-DIHYDROXYOCTANE
(2R)-octane-1,2-diol
(2S)-octane-1,2-diol
(R,S)-Octane-1,2-diol
CAS 1117-86-8
EINECS 214-254-7
InChI InChI=1/C8H18O2/c1-2-3-4-5-6-8(10)7-9/h8-10H,2-7H2,1H3/t8-/m0/s1

Physico-chemical Properties

Molecular Formula C8H18O2
Molar Mass 146.23
Density 0.914
Melting Point 36-38 °C (lit.)
Boling Point 131-132 °C/10 mmHg (lit.)
Flash Point >230°F
Water Solubility 3 g/L (20 ºC)
Solubility 3 g/L (20°C)
Vapor Presure 0.28Pa at 25℃
Vapor Density >1 (vs air)
Appearance Transparent liquid
Color Colorless to white
BRN 1719619
pKa 14.60±0.10(Predicted)
Storage Condition Sealed in dry,Room Temperature
Refractive Index 1.4505 (estimate)
MDL MFCD00010738

Risk and Safety

Hazard Symbols Xi - Irritant
Irritant
Risk Codes 36 - Irritating to the eyes
Safety Description S37/39 - Wear suitable gloves and eye/face protection
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S24/25 - Avoid contact with skin and eyes.
WGK Germany 2
TSCA Yes
HS Code 29053990
Hazard Class IRRITANT

Introduction

Solubility in water: 3g/L (20°C)

Reference Information

LogP 2.1 at 25℃
introduction 1, 2-octanediol is a colorless liquid or white solid, and its boiling point (℃) at 1330Pa is 131-132 ℃. 1, 2-octanediol can be mixed with a variety of organic chemicals in any proportion, and has good formula compatibility.
preparation to the reaction kettle equipped with stirring, thermometer and high-level tank, add formic acid and hydrogen peroxide, start stirring, then add 1-octene, after adding, the reaction mixture solution continues to be maintained for 100 minutes, then the formic acid and water are evaporated under reduced pressure, and then the sodium hydroxide solution is added under stirring until the PH value of the mixture solution is alkaline, then the ester is added for extraction, and the obtained extract is washed twice with sodium chloride with a concentration of 30%. The washed extract is dehydrated with anhydrous magnesium sulfate and then distilled under reduced pressure. The fraction is collected under the condition of 131 ℃/1330Pa. The resulting fraction is the product 1, 2-octanediol.

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