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Sigma-Aldrich

α-Pinene

98%

Synonym(s):

alpha-Pinene, (±)-2-Pinene, 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene

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About This Item

Empirical Formula (Hill Notation):
C10H16
CAS Number:
80-56-8
Molecular Weight:
136.23
EC Number:
201-291-9
MDL number:
MFCD00001339
UNSPSC Code:
12352100
PubChem Substance ID:
24848559
NACRES:
NA.22

Quality Level

100

Assay

98%

form

liquid

autoignition temp.

491 °F

refractive index

n20/D 1.465 (lit.)

bp

155-156 °C (lit.)

density

0.858 g/mL at 25 °C (lit.)

SMILES string

[H][C@@]12CC=C(C)[C@@]([H])(C1)C2(C)C

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

InChI key

GRWFGVWFFZKLTI-RKDXNWHRSA-N

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General description

α-Pinene is a chemical constituent of essential oil extracted from the stem of Canarium tramdenanum.
It reacts with ozone in the air to form oxygenated products that can further react to form secondary organic aerosols (SOA).

Application

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.

Signal Word

Danger

Hazard Statements

H226,H304,H315,H317,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

87.8 °F - closed cup

Flash Point(C)

31 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Newly characterized products and composition of secondary aerosols from the reaction of ?-pinene with ozone.
Jang M and Kamens R M
Atmospheric Environment, 33(3), 459-474 (1999)
Aerosol formation from the reaction of ?-pinene and ozone using a gas-phase kinetics-aerosol partitioning model.
Kamens R, et al.
Environmental Science & Technology, 33(9), 1430-1438 (1999)
Structure-activity relations in Cs-doped heteropolyacid catalysts for biodiesel production.
Narasimharao K, et al.
J. Catal., 248(2), 226-234 (2007)
Jeremy D Allison et al.
Environmental entomology, 41(6), 1587-1596 (2013-01-17)
In recent years, several attractant pheromones have been identified for cerambycid beetles, including 2-(undecyloxy)-ethanol (hereafter monochamol) for Monochamus galloprovincialis (Olivier), M. alternatus Hope, and M. scutellatus (Say). This study screened eight known cerambycid pheromones or their analogues (including monochamol) as
Aleksandra Zielińska et al.
Pharmaceutical development and technology, 25(7), 832-844 (2020-03-25)
Glycerol monostearate solid lipid nanoparticles (SLN) were produced by hot high-pressure homogenization technique to load alpha-pinene, citral, geraniol or limonene. SLN were composed of 1 wt.% monoterpene, 4 wt.% of Imwitor® 900K as a solid lipid and 2.5 wt.% of Poloxamer188 as a
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Protocols

Sweet Orange Essential Oil GC Analysis

Fast GC analysis of sweet orange essential oil in hexane. Key components identified includes: β-Farnesene; α-Huµlene; Germacrene D; (+)-Valencene; Bicyclogermacrene; (+)-δ-Cadinene

Chromatograms

suitable for GCsuitable for GCsuitable for GC

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