Uses application
ChemicalBook > CAS DataBase List > 1,2-Octanediol

1,2-Octanediol

Uses application
Product Name
1,2-Octanediol
CAS No.
1117-86-8
Chemical Name
1,2-Octanediol
Synonyms
CAPRYLYL GLYCOL;Octane-1,2-diol;1,2-DIHYDROXYOCTANE;octane-1,;1,2-Octandiol;Octan-1,2-diol;1,2-OCTANEDIOL;1,2-OCLanediol;1,2-0ctanediol;n-Octane-1,2-diol
CBNumber
CB8747116
Molecular Formula
C8H18O2
Formula Weight
146.23
MOL File
1117-86-8.mol
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1,2-Octanediol Property

Melting point:
36-38 °C (lit.)
Boiling point:
131-132 °C/10 mmHg (lit.)
Density 
0.914
vapor density 
>1 (vs air)
vapor pressure 
0.28Pa at 25℃
refractive index 
1.4505 (estimate)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
3 g/L (20°C)
form 
Low Melting Solid
pka
14.60±0.10(Predicted)
color 
Colorless to white
Water Solubility 
3 g/L (20 ºC)
BRN 
1719619
LogP
2.1 at 25℃
CAS DataBase Reference
1117-86-8(CAS DataBase Reference)
NIST Chemistry Reference
1,2-Octanediol(1117-86-8)
EPA Substance Registry System
1,2-Octanediol (1117-86-8)
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Safety

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
37/39-26-24/25
WGK Germany 
2
TSCA 
Yes
HazardClass 
IRRITANT
HS Code 
29053990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H319Causes serious eye irritation

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P337+P313IF eye irritation persists: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
213705
Product name
1,2-Octanediol
Purity
98%
Packaging
10g
Price
$30.1
Updated
2024/03/01
Sigma-Aldrich
Product number
213705
Product name
1,2-Octanediol
Purity
98%
Packaging
50g
Price
$106
Updated
2024/03/01
TCI Chemical
Product number
O0277
Product name
1,2-Octanediol
Purity
>96.0%(GC)
Packaging
25g
Price
$48
Updated
2024/03/01
TCI Chemical
Product number
O0277
Product name
1,2-Octanediol
Purity
>96.0%(GC)
Packaging
400g
Price
$219
Updated
2024/03/01
Alfa Aesar
Product number
L08031
Product name
1,2-Octanediol, 97%
Packaging
10g
Price
$25.65
Updated
2024/03/01
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1,2-Octanediol Chemical Properties,Usage,Production

Uses

1,2-Octanediol has a variety of applications. It is used to improve HPLC separation of organic acids and bases and to synthesize halohydrin palmitates. Additionally, it is studied for its potential use as a pediculicide and has been shown to be effective against louse infestations.

application

Diols contribute to high water solubility, hygroscopicity and reactivity with many organic compounds, on usually linear and aliphatic carbon chain. 1,2-Octanediol, linear diol containing two primary hydroxyl groups, has bacteriostatic and bacteriacidal properties which are useful in cosmetics as a preservative. It is also used in coating materials, slurries, paper mills and water circulation systems for the effective preservation against bacteria and fungi. It is used as an emollient, humectant, and wetting agent in cosmetic and skin care products. Alcohols are very weak acids as they lose H+ in the hydroxyl group. Alcohols undergoes dehydration reaction which means the elimination of water molecule replaced by a pi bond between two adjacent carbon atoms to form alkenes under heating in the presence of strong acids like hydrocloric acid or phosphoric acid. Primary and secondary alcohols can be oxidized to aldehydes and ketones respectively. Carboxylic acids are obtained from oxidation of aldehydes. Oxidation in organic chemistry can be considered to be the loss of hydrogen or gain of oxygen and reduction to gain hydrogen or loss of oxygen. Tertiary alcohols do not react to give oxidation products as they have no H attached to the alcohol carbon. Alcohols undergoes important reactions called nucleophilic substitution in which an electron donor replaces a leaving group, generally conjugate bases of strong acids, as a covalent substitute of some atom. One of important reaction of alcohol is condensation. Ethers are formed by the condensation of two alcohols by heating with sulfuric acid; the reaction is one of dehydration. Almost infinite esters are formed through condensation reaction called esterification between carboxylic acid and alcohol, which produces water. Alcohols are important solvents and chemical raw materials. Alcohols are intermediates for the production of target compounds, such as pharmaceuticals, veterinary medicines, plasticizers, surfactants, lubricants, ore floatation agents, pesticides, hydraulic fluids, and detergents.

Chemical Properties

colorless to white low melting solid

Uses

caprylyl glycol (1,2-Octanediol) is an emollient with moisturizing properties that may also be used as a cosmetic stabilizer. When found in combination with phenoxyethanol these two ingredients work together as an anti-microbial.

Uses

1,2-Octanediol is a novel surfactant used in the treatment of head louse. Also used in the cosmetics industry in the formulations of sunscreen gels and eye make-up.

Definition

ChEBI: Octane-1,2-diol is an octanediol.

Production Methods

1,2-octanediol could be obtained by epoxidation of 1-olefin with performic acid, a reaction product of hydrogen peroxide and formic acid, hydroxylation with water, or transesterification of ester produced by side reaction with methanol.

General Description

1,2-Octanediol is a potential pediculicide and is useful for treating head louse infestation clinically.

Purification Methods

Distil the diol in vacuo and/or recrystallise it from pet ether. The -naphthylurethane has m 112-114o. [Beilstein 1 III 2217, 1 IV 2590.] S-(-)-Octane-1,2-diol [87720-91-0] also crystallises from pet ether with m 35-37o and [] D -4.7o (c 35, EtOH) [Sp.th et al. Chem Ber 66 598 1933]; R-(+)-octane-1,2-diol [87720-90-9] has similar properties but with a positive optical rotation.

1,2-Octanediol Preparation Products And Raw materials

Raw materials

Preparation Products

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1,2-Octanediol Suppliers

wenzhou shoucheng
Tel
15102776735 15102776735
Fax
15102776735
Email
793269788@qq.com
Country
China
ProdList
35
Advantage
58
Shanghai GaoLang Chemical Technology Co., Ltd.
Tel
021-57340939 18017297327
Fax
021-37210791
Email
sales@gaolangchemical.com
Country
China
ProdList
892
Advantage
55
Nanjing LuoDa Chemical Co., Ltd
Tel
025-66016961 13382082786
Fax
025-52204547
Country
China
ProdList
288
Advantage
55
ZLEY (Guangzhou) Biological Research Co., Ltd
Tel
13295180996
Email
599930365@qq.com
Country
China
ProdList
30
Advantage
58
Huzhou Jiasi Biological Technology Co., Ltd.
Tel
18667213966
Email
jarvis.d@jiasibio.com
Country
China
ProdList
26
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94657
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Ark Pharm, Inc.
Tel
847-367-3680
Fax
847-367-3681
Email
sales@arkpharminc.com
Country
United States
ProdList
1670
Advantage
56
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View Lastest Price from 1,2-Octanediol manufacturers

Hebei Longbang Technology Co., Ltd
Product
1,2-Octanediol 1117-86-8
Price
US $6.00/kg
Min. Order
1kg
Purity
More than 99%
Supply Ability
2000KG/Month
Release date
2024-05-07
Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
1,2-Dihydroxyoctane 1117-86-8
Price
US $60.00/kg
Min. Order
1kg
Purity
99
Supply Ability
5000
Release date
2024-05-15
Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
1,2-Octanediol 1117-86-8
Price
US $100.00/kg
Min. Order
1kg
Purity
99
Supply Ability
5000
Release date
2024-04-23

1117-86-8, 1,2-OctanediolRelated Search:


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