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115576

Sigma-Aldrich

3-Carene

90%

Synonym(s):

δ3-Carene, 3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene

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About This Item

Empirical Formula (Hill Notation):
C10H16
CAS Number:
Molecular Weight:
136.23
EC Number:
MDL number:
UNSPSC Code:
12352212
PubChem Substance ID:
NACRES:
NA.22

Assay

90%

optical activity

[α]20/D +15°, neat

impurities

5% 2-carene

refractive index

n20/D 1.474 (lit.)

bp

168-169 °C/705 mmHg (lit.)

density

0.857 g/mL at 25 °C (lit.)

SMILES string

CC1=CCC2C(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

InChI key

BQOFWKZOCNGFEC-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

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

Certificates of Analysis (COA)

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Min Lu et al.
Ecology, 92(11), 2013-2019 (2011-12-15)
Novel genotypes often arise during biological invasions, but their role in invasion success has rarely been elucidated. Here we examined the population genetics and behavior of the fungus, Leptographium procerum, vectored by a highly invasive bark beetle, Dendroctonus valens, to
Yan Ma et al.
Physical chemistry chemical physics : PCCP, 11(21), 4184-4197 (2009-05-22)
This paper describes experimental studies aimed at elucidating mechanisms for the formation of low-volatility organic acids in the gas-phase ozonolysis of 3-carene. Experiments were carried out in a static chamber under 'OH-free' conditions. A range of multifunctional acids-which are analogous
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
Dawn E Hall et al.
The Plant journal : for cell and molecular biology, 65(6), 936-948 (2011-02-18)
Conifers are extremely long-lived plants that have evolved complex chemical defenses in the form of oleoresin terpenoids to resist attack from pathogens and herbivores. In these species, terpenoid diversity is determined by the size and composition of the terpene synthase
Smail Aazza et al.
Molecules (Basel, Switzerland), 16(9), 7672-7690 (2011-09-09)
The commercial essential oils of Citrus aurantium L., Cupressus sempervirens L., Eucalyptus globulus Labill., Foeniculum vulgare Mill. and Thymus vulgaris L., isolated by steam distillation by a company of Morocco were evaluated in terms of in vitro antioxidant activity through

Protocols

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

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