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alpha-Pinene

CAS No.
80-56-8
Chemical Name:
alpha-Pinene
Synonyms
PINENE;2-Pinene;2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene;Pin-2(3)-ene;Terpene hydrocarbon;2,6,6-trimethyl-bicyclo[3.1.1]hept-2-en;α-pinene,2,6,6-trimethylbicyclo[3.1.1]hept-2-ene;cyclicdexadiene;c 500;PC500;a-PINEE
CBNumber:
CB8209087
Molecular Formula:
C10H16
Molecular Weight:
136.23
MDL Number:
MFCD00001339
MOL File:
80-56-8.mol
MSDS File:
SDS
Last updated:2026-04-10 10:27:29
Product description Number Pack Size Price
D-Camphor Impurity A, a-pinene certified reference material, pharmaceutical secondary standard PHR2427 100MG $543
α-Pinene phyproof? Reference Substance PHL89257 100MG $347
alpha-Pinene solution certified reference material, 2000?μg/mL in methanol, ampule of 1?mL CRM40339 1mL $133
α-Pinene 98% 147524 1l $442
α-Pinene primary reference standard 00040590 100mg $506
More product size

alpha-Pinene Properties

Melting point -55°C
Boiling point 155-156 °C(lit.)
Density 0.858 g/mL at 25 °C(lit.)
vapor pressure 6.9hPa at 20℃
refractive index n20/D 1.465(lit.)
FEMA 2902 | ALPHA-PINENE
FLAVIS Number 01.004 | Pin-2(3)-ene
Flash point 90 °F
storage temp. 2-8°C
solubility Soluble in ethanol;
form Liquid
color Clear colorless
Odor at 10.00 % in dipropylene glycol. fresh camphor sweet pine earthy woody
Odor Threshold 0.018ppm
Odor Type herbal
Water Solubility insoluble
Merck 13,7527
JECFA Number 1329
Henry's Law Constant 7.0×10-5 mol/(m3Pa) at 25℃, Plyasunov and Shock (2000)
Dielectric constant 2.7(20℃)
Stability Stable. Flammable. Incompatible with strong oxidizing agents.
Cosmetics Ingredients Functions ANTIFOAMING
FRAGRANCE
InChI 1S/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h4,8-9H,5-6H2,1-3H3/t8-,9-/m1/s1
InChIKey GRWFGVWFFZKLTI-RKDXNWHRSA-N
SMILES [H][C@@]12CC=C(C)[C@@]([H])(C1)C2(C)C
LogP 4.46 at 20℃
CAS DataBase Reference 80-56-8(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS) ALPHA-PINENE
EWG's Food Scores 1
FDA UNII JPF3YI7O34
NIST Chemistry Reference «alpha»-Pinene(80-56-8)
EPA Substance Registry System .alpha.-Pinene (80-56-8)
UNSPSC Code 85151701
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07,GHS08,GHS09
Signal word  Danger
Hazard statements  H226-H304-H315-H317-H410
Precautionary statements  P210-P273-P280-P301+P310-P303+P361+P353-P331
PPE Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  Xi,N,Xn,F
Risk Statements  10-36/37/38-43-50-65-51/53-38-36/38-20
Safety Statements  26-36/37-61-37/39-29-16-36/37/39-7/9-62
RIDADR  UN 2368
WGK Germany  1
RTECS  DT7000000
Autoignition Temperature 491 °F
TSCA  TSCA listed
HazardClass  3
PackingGroup  III
HS Code  29021990
Storage Class 3 - Flammable liquids
Hazard Classifications Aquatic Acute 1
Aquatic Chronic 1
Asp. Tox. 1
Flam. Liq. 3
Skin Irrit. 2
Skin Sens. 1
Hazardous Substances Data 80-56-8(Hazardous Substances Data)
Limited Quantities 5.0 L (1.3 gallons) (liquid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L)
NFPA 704
3
1 0

alpha-Pinene price More Price(26)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHR2427 D-Camphor Impurity A, a-pinene certified reference material, pharmaceutical secondary standard 80-56-8 100MG $543 2026-03-19 Buy
Sigma-Aldrich PHL89257 α-Pinene phyproof? Reference Substance 80-56-8 100MG $347 2026-03-19 Buy
Sigma-Aldrich CRM40339 alpha-Pinene solution certified reference material, 2000?μg/mL in methanol, ampule of 1?mL 80-56-8 1mL $133 2026-03-19 Buy
Sigma-Aldrich 147524 α-Pinene 98% 80-56-8 1l $442 2026-03-19 Buy
Sigma-Aldrich 00040590 α-Pinene primary reference standard 80-56-8 100mg $506 2026-03-19 Buy
Product number Packaging Price Buy
PHR2427 100MG $543 Buy
PHL89257 100MG $347 Buy
CRM40339 1mL $133 Buy
147524 1l $442 Buy
00040590 100mg $506 Buy

alpha-Pinene Chemical Properties,Uses,Production

Description

Alpha-pinene is the major constituent of turpentine (about 80%). It exists as a levogyre form in European turpentines, and as a dextrogyre form in turpentines found in North America. Sensitization mainly occurs in painters, polishers and varnishers, and in those in the perfume and ceramics industry.

Chemical Properties

α-Pinene is the most widespread pinene isomer. (+)-α-Pinene, (1R,5R)-2,6,6-trimethylbicyclo[3.3.1]hept-2-ene, occurs, for example, in oil from Pinus palustris Mill., at a concentration up to 65%; oil from Pinus pinaster Soland and American oil from Pinus caribaea contain 70% and 70–80%, respectively, of the laevorotatory isomer, ()-α-Pinene, (1S,5S)-2,6,6-trimethylbicyclo[3.3.1]hept-2-ene.
α-Pinene undergoes many reactions, of which the following are used in the fragrance industry: upon hydrogenation, α-pinene is converted to pinane, which has become an important starting material in the industrial processes used in the fragrance and flavor industry. α-Pinene can be isomerized to β-pinene with high selectivity for β-pinene formation. Hydration with simultaneous ring opening yields terpineol and cis-terpin hydrate. Pyrolysis of α-pinene yields a mixture of ocimene and alloocimene.
Pure α-pinene is obtained by distillation of turpentine oils. As a fragrance substance, it is used to improve the odor of industrial products.However, it is farmore important as a starting material in industrial syntheses, for example, terpineols, borneol, and camphor.

Chemical Properties

liquid with a turpentine odour

Chemical Properties

α-Pinene has a characteristic odor of pine. It is turpentine-like. The oxidized material has a resin-like odor.

Occurrence

The structure would account for the presence of four optically active and two optically inactive isomers; although only d-, l-, and dl-α-pinene are known, however; presence of one or more isomers has been reported in more than 400 essential oils; in the largest amounts it has been reported found in Achillea millefolium (d-), Artemisia tridentata (d-), Italian rosemary (l-), wild thyme (l-), French lavender (l-), coriander (d-, dl-), cumin (d, dl-), labdanum (l-), neroli (l-), lemon, Litsea cubeba (d-) and ylang-ylang (d-). It is also reported in over 200 natural products including apple, apricot, many citrus juices and peel oils, bilberry, cranberry, lingonberry, blackberry, currants, guava, raspberry, strawberry, orange, lime, grapefruit, mandarin, tangerine oils and juices, various spices, mint essential oils, carrot, celery, cooked potato, bell pepper, tomato, anise, cinnamon, cassia leaf, clove, cumin, ginger, Mentha oils, nutmeg, mace, pepper, parsley, thyme, Swiss and cheddar cheese, cream, fatty fish, fried chicken, beef fat, hop oil, rum, bourbon whiskey, tea, roasted filberts, pecans, oats, soybean, plum, mushroom, sweet and wild marjoram, starfruit, mango, tamarind, cardamom, coriander, gin, rice, litchi, calamus, dill, lovage, caraway seed, buckwheat, laurel, fennel, kiwifruit, myrtle leaf and berry, rosemary, buchu oil, Bourbon vanilla, Spanish and clary sage, nectarine, crayfish, clam, cape gooseberry, anise hyssop, angelica root oil, Roman and German chamomile oil, eucalyptus oil, bullock’s heart and mastic gum leaf and fruit oil.

Uses

Reference Standard in the analysis of herbal medicinal products

Uses

α-Pinene was used as standard in headspace solid-phase microextraction-gas chromatographic analysis of volatile compounds in virgin olive oils. It was used in the synthesis of cesium-doped heteropolyacid having potential application in biodiesel synthesis.

Production Methods

α-Pinene occurs naturally in a variety of trees and shrubs, including more than 400 essential oils, and air concentrations near pine forests may reach 500–1200 mg/m3. Total U.S. emission of α-pinene from deciduous and coniferous forests amounts to 6.6 million tons annually. An estimated emission rate of α-pinene from natural sources to the atmosphere is 1.84×10 -10 g/cm3/s.

Preparation

From turpentine, by distillation.

Definition

ChEBI: A pinene that is bicyclo[3.1.1]hept-2-ene substituted by methyl groups at positions 2, 6 and 6 respectively.

Aroma threshold values

Detection: 2.5 to 62 ppb. Aroma characteristics at 1.0%: terpy citrus and spicy, woody pine and turpentinelike with a slight cooling camphoraceous nutmeglike nuance, a fresh herbal lift and a tropical fruit top note.

Taste threshold values

Taste characteristics at 10 ppm: intense, woody, piney and terpy with camphoraceous and turpentine notes. It has herbal, spicy and slightly tropical mango nuances.

General Description

A clear colorless liquid with a turpentine odor. Flash point 91°F. Less dense than water and insoluble in water. Vapors are heavier than air. Used as a solvent.

Air & Water Reactions

Highly flammable. Insoluble in water.

Reactivity Profile

alpha-Pinene may react vigorously with strong oxidizing agents. May react exothermically with reducing agents to release gaseous hydrogen.

Health Hazard

Harmful if swallowed, inhaled or absorbed through skin. High concentrations are extremely destructive to mucous membrane and upper respiratory tract, eyes and skin. Symptoms of exposure may include burning sensation, coughing, wheezing, laryngitis, shortness of breath, headache, nausea and vomiting.

Fire Hazard

Special Hazards of Combustion Products: Vapor may travel considerable distance to source of ignition and flashback. Container explosion may occur during fire conditions. Forms explosive mixtures in air.

Contact allergens

Alpha-pinene is the major constituent of turpentine (about 80%). It exists in levogyre form in European turpentine and in dextrogyre form in turpentine found in North-Americans. Sensitization occurs mainly in painters, polishers, and varnishers, and in those in the perfume and in the ceramics industry.

Safety Profile

A deadly poison by inhalation. Moderately toxic by ingestion. An eye, mucous membrane, and severe human skin irritant. Flammable liquid. A dangerous fire hazard when exposed to heat, flame, or oxidizing materials. To fight fire, use foam, Co2, dry chemical. Explodes on contact with nitrosyl perchlorate.

Toxics Screening Level

The ITSL for α-pinene is 1120 μg/m3 based on an 8-hour averaging time.

Global( 275)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Chuanghai Biotechnology Co., Ltd
+8615350571055 Sibel@chuanghaibio.com China 8738 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21592 55
Anhui Royal Chemical Co., Ltd.
+86-025-86655873 +86-13962173137 marketing@royal-chem.com China 201 55
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29821 58
Chengdu GLP biotechnology Co Ltd
028-87075086 13350802083 scglp@glp-china.com CHINA 1824 58
Chengdu Biopurify Phytochemicals Ltd.
+86-28-82633860; +8618080483897 sales@biopurify.com China 3751 58
Jinan Finer Chemical Co., Ltd
+86-531-88989536 +86-15508631887 sales@finerchem.com China 2949 58
NanJing Spring & Autumn Biological Engineering CO., LTD.
+8613815430202 sale02@cqherb.com CHINA 376 58
Shandong chuangyingchemical Co., Ltd.
18853181302 sale@chuangyingchem.com CHINA 5906 58
Shanghai Standard Technology Co., Ltd.
18502101150 ft-sales@nature-standard.com CHINA 1923 58

View Lastest Price from alpha-Pinene manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
alpha-Pinene pictures 2026-03-20 alpha-Pinene
80-56-8
US $10.00 / KG 1KG 99% 100 mt Hebei Chuanghai Biotechnology Co., Ltd
α-Pinene  pictures 2023-02-24 α-Pinene
80-56-8
US $0.00 / ml 0.1ml ≥90%(HPLC) 10 g Shanghai Standard Technology Co., Ltd.
α-Pinene 80-56-8 pictures 2022-02-14 α-Pinene 80-56-8
80-56-8
US $45.00 / mg 20mg >98% 1000.00 kgs NanJing Spring & Autumn Biological Engineering CO., LTD.
  • alpha-Pinene pictures
  • alpha-Pinene
    80-56-8
  • US $10.00 / KG
  • 99%
  • Hebei Chuanghai Biotechnology Co., Ltd
  • α-Pinene  pictures
  • α-Pinene
    80-56-8
  • US $0.00 / ml
  • ≥90%(HPLC)
  • Shanghai Standard Technology Co., Ltd.
  • α-Pinene 80-56-8 pictures
  • α-Pinene 80-56-8
    80-56-8
  • US $45.00 / mg
  • >98%
  • NanJing Spring & Autumn Biological Engineering CO., LTD.
(±)-pin-2-ene ,6,6-Trimethyl-bicyclo[3.1.1]hept-2-ene 2,6,6-trimethylbicyclo-(3,1,1)-2-heptene 2,6,6-Trimethylbicyclo(3.1.1)-2-hept-2-ene 2,6,6-Trimethylbicyclo(3.1.1)-2-heptene pin-2-ene Terpene hydrocarbon α-pin-2-ene MOUNTING MEDIA POLYMOUNT MOUNTING MEDIA PERMANENT MOUNTING MEDIA PERMOUNT PERMOUNT MOUNTING MEDIA alpha-Pinene, pract., 70% α-pinene,2,6,6-trimethylbicyclo[3.1.1]hept-2-ene;cyclicdexadiene PINANE, (1R)-(+)-cis(SG) PINANE, (1R)-(+)-trans(SG) PINANE, (1S)-(-)-trans(SG) PINANE, (1S)-(-)-cis(SG) 2,6,6-trimethyl-bicyclo(3.1.1)hept-2-en 2,6,6-trimethylbicyclo[3,1,1]-2-heptene (alpha-pinene) 2,6,6-trimethylbicyclo[3,1,1]-heptene (alpha-pinene) 2,6,6-trimethyl-bicyclo[3.1.1]hept-2-en 4,6,6-Trimethylbicyklo(3,1,1)hept-3-en AciteneA c 500 femanumber2902 PC500 alpha-Pinene(ACN) 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene 2-Pinene Pin-2(3)-ene alpha-PINENE, NATURAL a-Pinen (cf. terpene) Alpha-pinene, 97%, stabilized with alpha- tocopherol PINENE (±)-2-Pinene, 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene alpha-Pinene alpha-Pinene, stabilized with alpha-Tocopherol 2,6,6-Trimethylbicyclo[3.1.1]heptane-2-ene Australene Pina-2-ene alpha-Pinene,70%,pract. 2,6,6-Trimethylbicyclo[3,1,1]-2-hepte alpha-Pinene, stabilized with alpha-Tocopherol, 97% 250GR alpha-Pinene, stabilized with alpha-Tocopherol, 97% 5GR alpha-Pinene solution α-Pinene 80-56-8 JACS-80-56-8 2-Pinene,(±)-2-Pinene, 2,6,6-Trimethylbicyclo[3.1.1]Hept-2-Ene, Alpha-Pinene a-Pinene Solution alpha-Pinene,98% a-PINEE α-Pinene 98% 2H3]-α-Pinene 2,6,6-trimethylbicyclo[3.1.1]hept-2-ene (α-pinene) Alpha Pinene Nat (+/-)-alpha-Pinene