cyclooctanol

cyclooctyl alcohol

CAS: 696-71-9 C8 H16 O MW: 128.21472000

Identification

Namecyclooctanol
CAS Number696-71-9
EINECS211-800-6
FDA UNIISearch
Molecular FormulaC8 H16 O
Molecular Weight128.21472000
MDL NumberMFCD00001744
Nikkaji NumberJ31.679B
Beilstein1848166
XlogP31.60 (est)

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 25.10 °C. @ 760.00 mm Hg
Boiling Point 203.20 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.100000 mmHg @ 25.00 °C. (est)
Flash Point 187.00 °F. TCC ( 86.10 °C. ) (est)
logP (o/w) 2.470 (est)
Soluble in water, 1752 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for cyclooctanol usage levels up tonot for fragrance use.
Recommendation for cyclooctanol flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

found in nature

Synonyms

cyclooctyl alcohol Google Patents: Process for the preparation of cyclooctanol PubMed: Reactivity of Cyclanols Towards Quinaldinium Fluorochromate Oxidation. PubMed: Efficient catalytic cycloalkane oxidation employing a "helmet" phthalocyaninato iron(III) complex. PubMed: Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-induced cyclizations. PubMed: Disentangling the secondary relaxations in the orientationally disordered mixed crystals: cycloheptanol + cyclooctanol two-component system. PubMed: Dielectric and calorimetric study of orientationally disordered phases in two unusual two-component systems. PubMed: Thermodynamics of the molecular and chiral recognition of cycloalkanols and camphor by modified beta-cyclodextrins possessing simple aromatic tethers. PubMed: Switching of a macromolecular helicity for visual distinction of molecular recognition events. PubMed: Metabolic studies with nonnutritive sweeteners cyclooctylsulfamate and 4-methylcyclohexylsulfamate.