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About This Item
Linear Formula:
C6H10(CH2OH)2
CAS Number:
Molecular Weight:
144.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-268-9
Beilstein/REAXYS Number:
1902271
MDL number:
Assay:
99%
InChI key
YIMQCDZDWXUDCA-UHFFFAOYSA-N
InChI
1S/C8H16O2/c9-5-7-1-2-8(6-10)4-3-7/h7-10H,1-6H2
SMILES string
OCC1CCC(CO)CC1
vapor density
5 (vs air)
assay
99%
autoignition temp.
584 °F
bp
283 °C (lit.)
functional group
hydroxyl
Quality Level
Related Categories
General description
1,4-Cyclohexanedimethano is extensively used as cross-linking reagent in polymer industry.
Application
1,4-Cyclohexanedimethanol has been used in the synthesis of polyketal copolymers. It was used as diol comonomer during the synthesis of polyester-carbonates based on 1,3-propylene-co-1,4-cyclohexanedimethylene succinate.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
321.8 °F - closed cup
flash_point_c
161 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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Zehong Xiang et al.
Macromolecular bioscience, 19(8), e1900112-e1900112 (2019-06-22)
Inflammation-associated thrombosis is a non-negligible source of mortalities and morbidities worldwide. To manipulate inflammation-associated coagulation, nanoparticles that contain anti-inflammatory polymer (copolyoxalate containing vanillyl alcohol, PVAX) and anti-thrombotic heparin derivative deoxycholic acid (Hep-DOCA) are prepared. The strategy takes advantage of the
Single-step conversion of dimethyl terephthalate into cyclohexanedimethanol with Ru5PtSn, a trimetallic nanoparticle catalyst.
Ana B Hungria et al.
Angewandte Chemie (International ed. in English), 45(29), 4782-4785 (2006-06-24)
Alexandre Trogé et al.
The Journal of the Acoustical Society of America, 128(5), 2704-2714 (2010-11-30)
This paper describes the acoustic properties of a range of epoxy resins prepared by photocuring that are suitable for application in piezoelectric ultrasonic transducer matching layers. Materials, based on blends of diglycidyl ether of Bisphenol A and 1,4-cyclohexanedimethanol diglycidyl ether
Mingliang Ding et al.
Biodegradation, 23(1), 127-132 (2011-07-07)
Enzymatic hydrolytic degradation of polybutylene succinate (PBS), poly(polybutylenesuccinate-co-1,4-cyclohexane dimethanol) (PBS/CHDM) and poly(polybutylene succinate-co-diglycolic acid) (PBS/DGA) in mixed solvent of tetrahydrofuran (THF) and toluene was examined. Lipase was used as catalyst to degrade polymers with molecular weight of more than 100,000
New biodegradable polymers from renewable sources: Polyester-carbonates based on 1, 3-propylene-co-1, 4-cyclohexanedimethylene succinate.
Liu Y, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 39(14), 2508-2519 (2001)
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