Skip to Content
Merck
All Photos(1)

Documents

21986

Supelco

(+)-3-Carene

analytical standard

Synonym(s):

(1S)-3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C10H16
CAS Number:
Molecular Weight:
136.23
Beilstein:
1902767
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

Assay

≥98.5% (sum of enantiomers, GC)

form

liquid

optical activity

[α]20/D +17±1°, neat

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

color

clear

refractive index

n20/D 1.473

bp

170-172 °C (lit.)

density

0.864 g/mL at 20 °C (lit.)

application(s)

food and beverages

format

neat

SMILES string

CC1=CC[C@@H]2[C@H](C1)C2(C)C

InChI

1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h4,8-9H,5-6H2,1-3H3/t8-,9+/m1/s1

InChI key

BQOFWKZOCNGFEC-BDAKNGLRSA-N

Looking for similar products? Visit Product Comparison Guide

General description

3-Carene is a bicyclic monoterpene, occurring naturally in pine trees.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Signal Word

Danger

Hazard Statements

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)

116.6 °F - closed cup

Flash Point(C)

47 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Thomas Müller et al.
Environmental science and pollution research international, 11(3), 152-157 (2004-07-21)
Composting facilities are known to release odorous volatiles due to biodegradation of municipal waste and plant residues. Although odour perception and its grading is influenced by experience, attitude and adaptation, these emissions have created a lack of acceptance for residents
Inheritance of 3-carene concentration in Pinus monticola.
Hanover WJ.
Forest Science, 12(4), 447-450 (1966)
Curtis A Gray et al.
PloS one, 10(9), e0135752-e0135752 (2015-09-04)
The tree-killing mountain pine beetle (Dendroctonus ponderosae Hopkins) is an important disturbance agent of western North American forests and recent outbreaks have affected tens of millions of hectares of trees. Most western North American pines (Pinus spp.) are hosts and
Huijing Li et al.
Current biology : CB, 30(22), 4432-4440 (2020-09-19)
Finding a suitable oviposition site is a challenging task for a gravid female fly, because the hatched maggots have limited mobility, making it difficult to find an alternative host. The oriental fruit fly, Bactrocera dorsalis, oviposits on many types of
Ta-Jung Lu et al.
The Journal of organic chemistry, 76(6), 1621-1633 (2011-02-11)
A novel carene-based alanine-equivalent tricyclic iminolactone 16 has been synthesized via stereoselective dihydroxylation of the double bond, IBX oxidation of the secondary alcohol, esterification of the tertiary alcohol, deprotection of the resulting ester, and subsequent cyclization from commercially available (1S)-(+)-3-carene

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