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Merck

125598

Sigma-Aldrich

1,4-Cyclohexanedimethanol

mixture of cis and trans, 99%

Sinónimos:

1,4-Bis(hydroxymethyl)cyclohexane, mixture of cis and trans

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About This Item

Fórmula lineal:
C6H10(CH2OH)2
Número de CAS:
Peso molecular:
144.21
Beilstein/REAXYS Number:
1902271
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

5 (vs air)

Quality Level

assay

99%

autoignition temp.

584 °F

bp

283 °C (lit.)

functional group

hydroxyl

SMILES string

OCC1CCC(CO)CC1

InChI

1S/C8H16O2/c9-5-7-1-2-8(6-10)4-3-7/h7-10H,1-6H2

InChI key

YIMQCDZDWXUDCA-UHFFFAOYSA-N

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.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

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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Stephen C Yang et al.
Bioconjugate chemistry, 19(6), 1164-1169 (2008-05-27)
Acute inflammatory diseases are a major cause of death in the world, and effective treatments are greatly needed. Macrophages play a central role in causing acute inflammatory diseases, and there is currently great interest in developing drug delivery vehicles that
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)
Pu Wang et al.
Biomaterials science, 6(5), 1262-1270 (2018-04-17)
One of the major challenges in anticancer therapy is the poor penetration of anticancer drugs into tumors, especially in solid tumors, resulting in decreased therapeutic efficacy in vivo. To solve some of these problems, in this study, a dual-responsive polymeric
S L Sendelbeck et al.
Drug metabolism and disposition: the biological fate of chemicals, 13(3), 291-295 (1985-05-01)
Disposition of the 14C-labeled bioerodible polymer poly(2,2-dioxy-cis,trans-1,4-cyclohexane dimethylene tetrahydrofuran) (ALZAMER C101ct) and its ultimate hydrolysis products, 4-hydroxybutyrate (4HB) and cis,trans-1,4-bis(hydroxymethyl)cyclohexane (CHDM), was assessed in vivo in rats 24 hr after sc administration of the 14C-labeled polymer or hydrolysis products. The

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