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O3303

Sigma-Aldrich

1,8-Octanediol

98%

Synonym(s):

Octamethylene glycol

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About This Item

Linear Formula:
HO(CH2)8OH
CAS Number:
Molecular Weight:
146.23
Beilstein:
1633499
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

bp

172 °C/20 mmHg (lit.)

mp

57-61 °C (lit.)

SMILES string

OCCCCCCCCO

InChI

1S/C8H18O2/c9-7-5-3-1-2-4-6-8-10/h9-10H,1-8H2

InChI key

OEIJHBUUFURJLI-UHFFFAOYSA-N

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Application

1,8-Octanediol can undergo:
  • Polycondensation with citric acid to form biodegradable poly(1,8-octanediol citrate)(POC) crosslinked bioelastomer which can be blended with various additives.
  • Fischer esterification with dicarboxylic acids to form diol-based macromers.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

248.0 °F - closed cup

Flash Point(C)

120 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Kai-Hee Huong et al.
International journal of biological macromolecules, 116, 217-223 (2018-05-04)
Long carbon chain alkanediols are used in the production of poly(3-hydroxybutyrate-co-4-hydroxybutyrate) [P(3HB-co-4HB)], however these substrates possess high toxicity towards bacterial cells. This study demonstrated the effective utilisation of a long carbon chain alkanediol, namely 1,8-octanediol, to enhance the yield and
Alexander M Tatara et al.
Biomacromolecules, 18(6), 1724-1735 (2017-05-11)
In this work, we describe the synthesis and characterization of variants of poly(diol fumarate) and poly(diol fumarate-co-succinate). Through a Fischer esterification, α,ω-diols and dicarboxylic acids were polymerized to form aliphatic polyester comacromers. Because of the carbon-carbon double bond of fumaric
Synthesis and Characterization of Diol-Based Unsaturated Polyesters: Poly (diol fumarate) and Poly (diol fumarate-co-succinate).
Tatara AM, et al.
Biomacromolecules, 18(6), 1724-1735 (2017)
Chitin nanocrystal enhanced wet adhesion performance of mussel-inspired citrate-based soft-tissue adhesive.
Xu Y, et al.
Carbohydrate Polymers, 190, 324-330 (2018)
Alessandro Pellis et al.
Nature communications, 10(1), 1762-1762 (2019-04-18)
Following concerns over increasing global plastic pollution, interest in the production and characterization of bio-based and biodegradable alternatives is rising. In the present work, the synthesis of a series of fully bio-based alternatives based on 2,4-, 2,5-, and 2,6-pyridinedicarboxylic acid-derived

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