Online Database of Chemicals from Around the World

Cineole
[CAS# 470-82-6]

List of Suppliers
Baoji Herbest Bio-tech Co., Ltd. China Inquire  
+86 (917) 888-1635
root@herbest.cn
QQ chat
Chemical manufacturer since 2008
chemBlink standard supplier since 2008
Simagchem Corporation China Inquire  
+86 13806087780
sale@simagchem.com
Chemical manufacturer since 2002
chemBlink standard supplier since 2008
HBCChem, Inc. USA Inquire  
+1 (510) 219-6317
sales@hbcchem-inc.com
Chemical manufacturer
chemBlink standard supplier since 2008
Discovery Fine Chemicals Ltd. UK Inquire  
+44 (1202) 874-517
pjc@discofinechem.com
Chemical manufacturer
chemBlink standard supplier since 2009
Extrasynthese Chemical S.A.S. France Inquire  
+33 (47) 898-2034
info@extrasynthese.com
Chemical manufacturer
chemBlink standard supplier since 2009
BOC Sciences USA Inquire  
+1 (631) 485-4226
info@bocsci.com
Chemical manufacturer
chemBlink standard supplier since 2010
Aktin Chemicals Inc China Inquire  
+86 400-028-7725
info@aktinchem.com
QQ chat
Chemical manufacturer
chemBlink standard supplier since 2011
Shanghai Yuanye Bio-Technology Co., Ltd. China Inquire  
+86 (21) 6184-5781
+86 13585604150
shyysw053@163.com
QQ chat
Chemical manufacturer since 2009
chemBlink standard supplier since 2016
Complete supplier list of Cineole
Identification
Classification Chemical reagent >> Organic reagent >> Epoxide
Name Cineole
Synonyms 1,3,3-Trimethyl-2-oxabicyclo[2.2.2]octane; 1,8-Cineole; 1,8-Epoxy-p-menthane; 1,8-Oxido-p-menthane; Eucalyptol
Molecular Structure CAS # 470-82-6, Cineole, 1,3,3-Trimethyl-2-oxabicyclo[2.2.2]octane, 1,8-Cineole, 1,8-Epoxy-p-menthane, 1,8-Oxido-p-menthane, Eucalyptol
Molecular Formula C10H18O
Molecular Weight 154.25
CAS Registry Number 470-82-6
EC Number 207-431-5
FEMA 2465
SMILES CC1(C2CCC(O1)(CC2)C)C
Properties
Density 0.9±0.1 g/cm3, Calc.*, 0.928 g/mL (Expl.)
Melting point 1 ºC (Expl.)
Index of Refraction 1.461, Calc.*, 1.456 (Expl.)
Boiling Point 174.0±8.0 ºC (760 mmHg), Calc.*, 176 � 177 ºC (Expl.)
Flash Point 50.9±15.3 ºC, Calc.*, 49 ºC (Expl.)
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol symbol   GHS02;GHS07 Warning    Details
Hazard Statements H226-H317    Details
Precautionary Statements P210-P233-P240-P241-P242-P243-P261-P272-P280-P302+P352-P303+P361+P353-P321-P333+P317-P362+P364-P370+P378-P403+P235-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Flammable liquidsFlam. Liq.3H226
Skin sensitizationSkin Sens.1BH317
Skin sensitizationSkin Sens.1H317
Eye irritationEye Irrit.2H319
Flammable liquidsFlam. Liq.2H225
Acute toxicityAcute Tox.4H302
Skin irritationSkin Irrit.2H315
Serious eye damageEye Dam.1H318
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Respiratory sensitizationResp. Sens.1BH334
Aspiration hazardAsp. Tox.1H304
Specific target organ toxicity - repeated exposureSTOT RE2H373
Specific target organ toxicity - single exposureSTOT SE3H335
Specific target organ toxicity - single exposureSTOT SE2H371
Transport Information UN 1993
SDS Available
up Discovory and Applicatios
Cineole, also known as eucalyptol, is a natural organic compound with a refreshing, minty aroma, predominantly found in eucalyptus oil. This monoterpene has been instrumental in traditional medicine and modern applications due to its distinctive properties and benefits.Cineole was first identified in the early 19th century by chemists extracting essential oils from the Eucalyptus globulus tree. Initially isolated through steam distillation, cineole emerged as the chief constituent of eucalyptus oil, constituting up to 90% of the oil's composition. The discovery marked the beginning of its extensive use in medicinal and industrial fields.

Cineole is renowned for its medicinal properties, particularly its role as a natural decongestant and expectorant. It helps alleviate symptoms of respiratory conditions such as asthma, bronchitis, and sinusitis by thinning mucus and facilitating easier breathing. Cineole's anti-inflammatory and antimicrobial characteristics also make it effective in treating respiratory infections and soothing irritated mucous membranes.

Cineole is a key ingredient in many over-the-counter cold remedies, including cough syrups, lozenges, and inhalants. Its pleasant aroma not only provides symptomatic relief but also enhances the patient�s comfort during illness.

In aromatherapy, cineole is celebrated for its invigorating scent and its ability to promote mental clarity and focus. Inhaling cineole can help reduce fatigue and boost mood, making it a popular choice for stress relief and cognitive enhancement. It is often used in diffusers and essential oil blends aimed at improving concentration and overall well-being.

Cineole's versatility extends to various industrial applications. It is utilized in the formulation of cleaning agents and air fresheners due to its potent disinfectant properties and refreshing fragrance. Its ability to act as a natural solvent and degreaser further enhances its value in these products, providing effective, eco-friendly cleaning solutions.

In the food industry, cineole is used as a flavoring agent to impart a minty, camphor-like taste to certain products. Its presence is notable in beverages, confectioneries, and culinary spices, where it adds a distinctive note to the overall flavor profile.

While cineole is generally safe for use in recommended quantities, excessive inhalation or ingestion can cause adverse effects such as nausea and vomiting. Therefore, it is essential to adhere to dosage guidelines in both medicinal and industrial applications.

References

Leita, B. A., Warden, A. C., Burke, N., O'Shea, M. S. and Trimm, D., 2010. Production of p-cymene and hydrogen from a bio-renewable feedstock�1,8-cineole (eucalyptus oil). Green Chemistry, 12, 70.
DOI: 10.1039/b916460j

Bhosle, D., Srinivasan, T., Elaiyabharathi, T., et al., 2025. A review on use of botanical extracts for the management of fall armyworm Spodoptera frugiperda (Smith, 1797) [Noctuidae, Lepidoptera]. J Plant Dis Prot, 132, 17.
DOI: 10.1007/s41348-024-01042-5

Obistioiu, D., Cristina, R. T., Schmerold, I., et al., 2014. Chemical characterization by GC-MS and in vitro activity against Candida albicans of volatile fractions prepared from Artemisia dracunculus, Artemisia abrotanum, Artemisia absinthium and Artemisia vulgaris. Chemistry Central Journal, 8, 6.
DOI: 10.1186/1752-153X-8-6
Market Analysis Reports
List of Reports Available for Cineole
Related Products
trans-Cinnamyl alcohol  Cinnamyl benzoate  Cinnamyl bromide  Cinnamyl butyrate  Cinnamyl chloride  Cinnamyl chloride  Cinnamyl cinnamate  Cinchonine hydrochloride  Cinchonine hydrochloride  Cincreasin  1,4-Cineole  Cinepazide  Cinepazide maleate  Cinitapride  Cinitapride Impurity 3  Cinitapride Impurity 7  Cinitapride Impurity 1 HCl  Cinitapride tartrate  Cinmethylin  Cinnabarinic acid