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alpha-Pinene
[CAS# 80-56-8]

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Complete supplier list of alpha-Pinene
Identification
Classification Chemical reagent >> Organic reagent >> Olefins (cyclic and non-cyclic)
Name alpha-Pinene
Synonyms 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene; 2-Pinene; Pin-2(3)-ene
Molecular Structure CAS # 80-56-8 (2437-95-8), alpha-Pinene, 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene, 2-Pinene, Pin-2(3)-ene
Molecular Formula C10H16
Molecular Weight 136.23
CAS Registry Number 80-56-8 (2437-95-8)
EC Number 201-291-9
SMILES CC1=CCC2CC1C2(C)C
Properties
Density 0.858
Melting point -55 ºC
Boiling point 154-157 ºC
Refractive index 1.465-1.467
Flash point 38 ºC
Water solubility insoluble
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315    Details
Precautionary Statements P264-P280-P302+P352-P321-P332+P317-P362+P364    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Flammable liquidsFlam. Liq.3H226
Skin irritationSkin Irrit.2H315
Aspiration hazardAsp. Tox.1H304
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Acute hazardous to the aquatic environmentAquatic Acute1H400
Skin sensitizationSkin Sens.1H317
Serious eye damageEye Dam.1H318
Acute toxicityAcute Tox.4H302
Skin sensitizationSkin Sens.1BH317
Eye irritationEye Irrit.2H319
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.4H312
Specific target organ toxicity - single exposureSTOT SE3H335
Acute toxicityAcute Tox.2H300
Acute toxicityAcute Tox.2H310
Acute toxicityAcute Tox.2H330
Flammable liquidsFlam. Liq.1H224
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Eye irritationEye Irrit.2BH320
Transport Information UN 2368
SDS Available
up Discovory and Applicatios
Alpha-pinene is a naturally occurring monoterpene that has attracted the attention of scientists and industry for its unique pine aroma and multiple uses since its discovery. Alpha-pinene was first isolated and identified from pine resin in the 19th century and is responsible for the characteristic smell of pine forests. It is one of the most common terpenes in nature and is found in the essential oils of conifers such as pine, fir and cedar. Its discovery marked the early recognition of terpenoid chemistry and its potential applications in perfumery and other fields.

Chemically, alpha-pinene belongs to the family of bicyclic monoterpenes, specifically a bicyclic hydrocarbon with two isomeric forms: alpha-pinene and beta-pinene. Alpha-pinene is characterized by its unique fresh, woody and resinous aroma, reminiscent of pine needles and forest air. This aromatic profile makes it a highly regarded ingredient in perfumery, used as a base note in masculine and outdoor-themed fragrances, adding depth and authenticity.

In perfumery, alpha-pinene enhances fragrance compositions by imparting a natural, outdoorsy scent, evoking feelings of freshness and vitality. It blends harmoniously with other aromatic compounds, contributing to the creation of fine fragrances and consumer products such as air fresheners, soaps and detergents. α-pinene�s ability to evoke memories of nature has made it a popular choice for products designed to recreate the sensory experience of the outdoors.

In addition to its aromatic properties, α-pinene has significant medicinal properties that have attracted attention in pharmacological research. It is an important ingredient in traditional and modern medicines due to its anti-inflammatory, bronchodilator and antimicrobial effects. α-pinene is actively studied for its potential in treating respiratory diseases and enhancing cognitive function through aromatherapy, highlighting its role in promoting health and well-being.

The versatility of α-pinene extends to industrial applications, where it is a precursor for a variety of chemicals and renewable materials. Through catalytic processes, α-pinene can be converted into compounds such as camphene and synthetic fragrances. In addition, α-pinene derivatives are used in the production of resins, adhesives and bio-based polymers, contributing to the development of sustainable materials with less environmental impact.

Challenges to commercializing α-pinene include optimizing extraction methods, ensuring a stable supply chain, and exploring environmentally friendly synthetic pathways to sustainably meet global demand. Ongoing research focuses on improving production efficiency and expanding the application of α-pinene in biotechnology and renewable energy, with the potential to make progress in biofuels and green chemistry.
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Related Products
(1S,2S,3R,5S)-(+)-2,3-Pinanediol  2-Pinanyl hydroperoxide  Pinanyl hydroperoxide  Pinaverium  Pinaverium bromide  Pindolol  Pine bark extract  beta-Pinene  (1R)-(+)-alpha-Pinene  (1S)-(1)-beta-Pinene  (1S)-(-)-alpha-Pinene  Pineneedle Oil  alpha-Pinene-isoprene copolymer  alpha-Pinene oxide  (+)-beta-Pinene oxide  2-Pinene, polymer with 2(10)-pinene  Pine oil  Pine Oil  Pine, Pinus pinaster, ext.  Pine tar