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402753

Sigma-Aldrich

(−)-β-Pinene

≥99%

Synonym(s):

(-)-beta-Pinene, (1S)-(−)-β-Pinene, (1S,5S)-2(10)-Pinene, (1S,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptane

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About This Item

Empirical Formula (Hill Notation):
C10H16
CAS Number:
18172-67-3
Molecular Weight:
136.23
Beilstein:
2038282
EC Number:
242-060-2
MDL number:
MFCD00001345
UNSPSC Code:
12352212
eCl@ss:
39011007
PubChem Substance ID:
24865115
NACRES:
NA.22

vapor density

4.7 (vs air)

vapor pressure

~2 mmHg ( 20 °C)

Assay

≥99%

form

liquid

optical activity

[α]25/D −22°, neat

optical purity

ee: 97% (GLC)

refractive index

n20/D 1.478 (lit.)

bp

165-167 °C (lit.)

mp

−61 °C (lit.)

density

0.866 g/mL at 25 °C

SMILES string

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

InChI

1S/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h8-9H,1,4-6H2,2-3H3/t8-,9-/m0/s1

InChI key

WTARULDDTDQWMU-IUCAKERBSA-N

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Application

(-)-β-Pinene has been used as a standard for the analysis of terpenoid compounds in plant essential oils by GC analysis. It may be used as a building block to synthesize natural products such as grandisol, robustadial and (+)-nopinone. (-)-β-Pinene undergoes hydroformylation in the presence of platinum/tin catalysts to form trans-10-formylpinane.

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)

102.2 °F - closed cup

Flash Point(C)

39 °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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Tetrahedron Letters, 30, 6653-6653 (1989)
Reduction of Legionella spp. in water and in soil by a citrus plant extract vapor.
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Applied and Environmental Microbiology, 80(19), 6031-6036 (2014)
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The continuous and indiscriminate use of insecticides has been responsible for the emergence of insecticide resistant vector insect populations, especially in Aedes aegypti. Thus, it is urgent to find natural insecticide compounds with novel mode of action for vector control.
Dual stereoselectivity in the dialkylzinc reaction using (-)-?-pinene derived amino alcohol chiral auxiliaries
Binder CM, et al
The Journal of Organic Chemistry, 74(6), 2337-2343 (2009)
Katie Laird et al.
Applied and environmental microbiology, 80(19), 6031-6036 (2014-07-27)
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