Skip to Content
Merck
All Photos(1)

Documents

305715

Sigma-Aldrich

(−)-α-Pinene

99%, optical purity ee: 97% (GLC)

Synonym(s):

(-)-alpha-Pinene, (1S)-(−)-α-Pinene, (1S,5S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene, (1S,5S)-2-Pinene

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C10H16
CAS Number:
Molecular Weight:
136.23
Beilstein:
1903790
EC Number:
MDL number:
UNSPSC Code:
12352002
eCl@ss:
39011007
PubChem Substance ID:
NACRES:
NA.22

vapor density

4.7 (vs air)

vapor pressure

~3 mmHg ( 20 °C)

Assay

99%

form

liquid

optical activity

[α]20/D −50.7°, neat

optical purity

ee: 97% (GLC)

autoignition temp.

491 °F

refractive index

n20/D 1.465 (lit.)

bp

155-156 °C (lit.)

mp

-64 °C (lit.)

density

0.855 g/mL at 25 °C

SMILES string

CC1=CCC2CC1C2(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-/m0/s1

InChI key

GRWFGVWFFZKLTI-IUCAKERBSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

(−)-α-Pinene can be used as a precursor for the preparation of:
  • Dichloro[(1R,2S,3R,5R)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]borane by the in situ reduction and hydroboration reaction.
  • α-Pinene oxide by epoxidation using polymer supported by a molybdenum carbonyl catalyst.
  • Diisopinocampheylborane (Ipc2BH), which is used for the asymmetric hydroboration prochiral alkenes.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 3 - Skin Irrit. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

88.3 °F

Flash Point(C)

31.3 °C

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Hydroboration. 93. Convenient Conversion of Optically Pure 2-Organylapopinenes into the (2-Organylapoisopinyl) dihaloboranes Potentially Valuable for Asymmetric Synthesis via Chiral Organoboranes
Dhokte UP and Brown HC
Organometallics, 15(16), 3504-3508 (1996)
Epoxidation of alkenes by a highly reusable and efficient polymer-supported molybdenum carbonyl catalyst
Grivani G, et al.
Catalysis Communications, 6(6), 375-378 (2005)
Versatile α-pinene-based borane reagents for asymmetric syntheses
Brown HC and Ramachandran PV
Journal of Organometallic Chemistry, 500(1-2), 1-19 (1995)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service