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Terpineol
[CAS# 8000-41-7]

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Complete supplier list of Terpineol
Identification
Classification Organic raw materials >> Hydrocarbon compounds and their derivatives >> Cyclic hydrocarbon
Name Terpineol
Synonyms 2-(4-Methyl-3-cyclohexenyl)-2-propanol; 1-Methyl-4-isopropyl-1-cyclohexen-8-ol; 4-Menth-1-en-8-ol
Molecular Structure CAS # 8000-41-7 (8006-39-1), Terpineol, 2-(4-Methyl-3-cyclohexenyl)-2-propanol, 1-Methyl-4-isopropyl-1-cyclohexen-8-ol, 4-Menth-1-en-8-ol
Molecular Formula C10H18O
Molecular Weight 154.25
CAS Registry Number 8000-41-7 (8006-39-1)
EC Number 201-196-2
SMILES CC1=CCC(CC1)C(C)(C)O
Properties
Density 0.937
Melting point 18 ºC
Boiling point 214-224 ºC
Refractive index 1.481-1.486
Flash point 95 ºC
Water solubility slightly
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319    Details
Precautionary Statements P264-P264+P265-P280-P302+P352-P305+P351+P338-P321-P332+P317-P337+P317-P362+P364    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Skin sensitizationSkin Sens.1H317
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Aspiration hazardAsp. Tox.1H304
Specific target organ toxicity - single exposureSTOT SE3H335
Reproductive toxicityRepr.2H361f
Serious eye damageEye Dam.1H319
Eye irritationEye Irrit.2AH319
Skin corrosionSkin Corr.1AH315
Acute toxicityAcute Tox.4H302
SDS Available
up Discovory and Applicatios
Terpineol is a naturally occurring monoterpene alcohol that was first isolated and identified from pine oil in the 19th century. It is found in various essential oils from plants such as pine, eucalyptus, clove and cannabis. It belongs to the terpene family, which has a unique aroma and biological activity. Chemically, terpineol exists in several isomeric forms, the most common being α-terpineol, β-terpineol and γ-terpineol, each with its own unique aroma and properties.

The chemical structure of terpineol includes a cyclic monoterpene backbone with an alcohol functional group, making it soluble in alcohol and oils while giving off a pleasant floral or pine aroma. The versatility of this structure allows terpineol to perform a variety of roles in a variety of applications, from enhancing scents to providing various therapeutic effects.

Terpineol is highly regarded in the fragrance industry for its ability to add depth and complexity to fragrance compositions. Its floral and citrus notes blend well with other aromatic compounds, making it a valuable ingredient in fine perfumes and consumer products such as cosmetics, soaps and detergents. In aromatherapy, terpineol is exploited for its calming effects, promoting relaxation and stress relief when used in essential oil blends or diffusers.

In addition to its aromatic properties, terpineol has various medicinal properties, making it a valuable ingredient in pharmaceutical formulations. It has antibacterial and antifungal properties, making it an effective treatment for skin infections and wounds. Terpineol's potential as an analgesic and anti-inflammatory agent has also been explored, highlighting its role in pain management and supportive care.

In industrial settings, terpineol can be used to formulate cleaning products, disinfectants, and air fresheners. Its pleasant scent not only masks bad odors, but also provides a natural alternative to synthetic chemicals, in line with consumer preferences for environmentally friendly and sustainable products. Terpineol's antimicrobial properties make it effective in household cleaners, ensuring an effective hygienic environment.

References

2024. Aroma Alchemy: Uridine diphosphate-dependent glycosyltransferases mediated regulation of fruit aroma and flavor biosynthesis. Phytochemistry Reviews.
DOI: 10.1007/s11101-024-10049-7

2024. A review on botany, ethnobotany, phytochemistry, ethnopharmacology and conservation status of Pinus gerardiana Wall. ex D. Don- The �elixir of life�. Genetic Resources and Crop Evolution.
DOI: 10.1007/s10722-024-02293-9

2024. Lactiplantibacillus plantarum postbiotics and thyme essential oil nanoemulsion-based edible spray: An innovative approach to extending shelf life of rainbow trout fillets. Journal of Food Measurement and Characterization.
DOI: 10.1007/s11694-024-03004-9
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Related Products
[1,1':4',1''-Terphenyl]-3,3'',5,5''-tetracarboxylic acid  (10-[1,1':3',1''-Terphenyl]-5'-yl-9-anthracenyl)boronic acid  [1,1':4',1''-Terphenyl]-2-ylboronic acid  B-[1,1':3',1''-Terphenyl]-3-ylboronic acid  B-[1,1':4',1''-Terphenyl]-4-ylboronic acid  9-([1,1':3',1''-Terphenyl]-4-yl)-9'-phenyl-9H,9'H-3,3'-bicarbazole  trans-Terpin  alpha-Terpinene  Terpinen-4-ol  (R)-Terpinen-4-ol  alpha-Terpineol  (-)-alpha-Terpineol  gamma-Terpineol  Terpineol acetate  Terpinolene  Terpinyl acetate  alpha-Terpinyl isobutyrate  Terpinyl thiocyanoacetate  2,2':6',2''-Terpyridine  [2,2':6',2''-Terpyridine]-4'-carboxylic acid