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C101206

Sigma-Aldrich

1,4-Cyclohexanediol

99%

Synonym(s):

Hexahydrohydroquinone

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About This Item

Linear Formula:
C6H10(OH)2
CAS Number:
556-48-9
Molecular Weight:
116.16
Beilstein:
2036658
EC Number:
209-126-2
MDL number:
MFCD00001448
UNSPSC Code:
12352100
PubChem Substance ID:
24892298
NACRES:
NA.22

Assay

99%

form

powder

bp

150 °C/20 mmHg (lit.)

mp

98-100 °C (lit.)

SMILES string

OC1CCC(O)CC1

InChI

1S/C6H12O2/c7-5-1-2-6(8)4-3-5/h5-8H,1-4H2

InChI key

VKONPUDBRVKQLM-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

149.0 °F - closed cup

Flash Point(C)

65 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Shuai Shuai Wu et al.
Cryo letters, 34(5), 497-507 (2014-01-23)
In this study, the fibroblasts cell line derived from ear marginal tissue of Yunnan semi-fine wool sheep was successfully established using the primary explants technique and cryopreservation technology. Additionally, the protective effect of synthetic ice blocker (SIB) including 1, 3-cyclohexanediol
Jun Wu et al.
Applied microbiology and biotechnology, 73(5), 1097-1105 (2006-09-16)
Commercial formulations of hexachlorocyclohexane (HCH) consist of a mixture of four isomers: alpha, beta, gamma, and delta. All four isomers are toxic and recalcitrant pollutants. beta-HCH is more problematic due to its longer persistence in the environment. Sphingomonas sp. BHC-A
G Giavaresi et al.
The International journal of artificial organs, 27(9), 796-805 (2004-11-04)
Two natural Biopol polyesters, containing 8% (D400G) and 12% (D600G) of hydroxyvalerate component, and a synthetic polyester based on 1,4 cyclohexanediol [Poly(cyclohexyl-sebacate)--PCS] were studied to investigate their in vitro and in vivo behavior for application in musculoskeletal tissue repair. The
Stéphane Patry et al.
Carbohydrate research, 500, 108217-108217 (2020-12-16)
In this paper, the synthesis of different bisglucosides is investigated through the reaction of two acetylated glucose units with a diol (or diphenol) in order to develop a versatile molecular platform for the future development of bio-based polymers. A panel
Nan Li et al.
International journal of pharmaceutics, 387(1-2), 167-171 (2009-12-23)
The objective of this study is to investigate the effect of 1,4-cyclohexanediol as a retardant on the percutaneous absorption and penetration of azelaic acid. Hairless rat skin was mounted on Franz diffusion cells and treated with topical formulations containing solubilized
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