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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

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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
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
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
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
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
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