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1,4-Cineole

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For Research Use Only | Not For Clinical Use
CATAP470677
CAS470-67-7
MDL NumberMFCD00209502
Molecular Weight154.25
EC Number207-428-9
InChI KeyRFFOTVCVTJUTAD-AOOOYVTPSA-N
REAXYS Number104974
Descriptionanalytical standard
Density0.887 g/mL at 25 °C (lit.)
Assay≥98.5% (GC)
BP65 °C/16 mmHg (lit.)
Formneat; gas chromatography (GC): suitable
Gradeanalytical standard
MP−46 °C (lit.)
Refractive Indexn20/D 1.445 (lit.); n20/D 1.445
Size1ML, 5ML
1

1,8- And 1,4-cineole Enhance Spontaneous Excitatory Transmission by Activating Different Types of Transient Receptor Potential Channels in the Rat Spinal Substantia Gelatinosa

Chang-Yu Jiang, Chong Wang, Nian-Xiang Xu, Tsugumi Fujita, Yuzo Murata, Eiichi Kumamoto

J Neurochem. 2016 Feb;136(4):764-777.

PMID: 26578070

1

Anxiolytic-like Effect of the Monoterpene 1,4-cineole in Mice

Patrícia Bezerra Gomes, Mariana Lima Feitosa, Maria Izabel Gomes Silva, Emmanuelle Coelho Noronha, Brinell Arcanjo Moura, Edith Teles Venâncio, Emiliano Ricardo Vasconcelos Rios, Damião Pergentino de Sousa, etc.

Pharmacol Biochem Behav. 2010 Sep;96(3):287-93.

PMID: 20670917

1

Investigation and Sensory Characterization of 1,4-Cineole: A Potential Aromatic Marker of Australian Cabernet Sauvignon Wine

Guillaume Antalick, Sophie Tempère, Katja Šuklje, John W Blackman, Alain Deloire, Gilles de Revel, Leigh M Schmidtke

J Agric Food Chem. 2015 Oct 21;63(41):9103-11.

PMID: 26434979

1

Microbial Hydroxylation of 1,4-cineole

J P Rosazza, J J Steffens, F S Sariaslani, A Goswami, J M Beale, S Reeg, R Chapman

Appl Environ Microbiol. 1987 Oct;53(10):2482-6.

PMID: 16347465

1

Selective Hydroxylation of 1,8- And 1,4-cineole Using Bacterial P450 Variants

Joel H Z Lee, Siew Hoon Wong, Jeanette E Stok, Sarah A Bagster, James Beckett, Jack K Clegg, Aidan J Brock, James J De Voss, Stephen G Bell

Arch Biochem Biophys. 2019 Mar 15;663:54-63.

PMID: 30590022

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