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275166

(+)-Sabinene

99%

Synonym(s):

(1R,5R)-1-Isopropyl-4-methylenebicyclo[3.1.0]hexane, (1R,5R)-4(10)-Thujene

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About This Item

Empirical Formula (Hill Notation):
C10H16
CAS Number:
2009-00-9
Molecular Weight:
136.23
Beilstein/REAXYS Number:
2038285
MDL number:
MFCD00010244
PubChem Substance ID:
329752999

assay

99%

bp

163-164 °C (lit.)

density

0.844 g/mL at 20 °C (lit.)

SMILES string

CC(C)[C@]12CCC(=C)[C@H]1C2

InChI

1S/C10H16/c1-7(2)10-5-4-8(3)9(10)6-10/h7,9H,3-6H2,1-2H3/t9-,10-/m1/s1

InChI key

NDVASEGYNIMXJL-NXEZZACHSA-N

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pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

96.8 °F - closed cup

flash_point_c

36 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
12120TV
10425CZ
02113DZ
08207TW

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L Chiappini et al.
Analytical and bioanalytical chemistry, 386(6), 1749-1759 (2006-09-15)
A new one-step method for the analysis of highly polar components of secondary organic aerosols (SOA) has been developed. This method should lead to a better understanding of SOA formation and evolution since it enables the compounds responsible for SOA
Lars Müller et al.
Rapid communications in mass spectrometry : RCM, 23(7), 971-979 (2009-02-27)
The components of secondary organic aerosols (SOAs) generated from the gas-phase ozonolysis of two C(10)H(16)-terpenes (alpha-pinene; sabinene) and a cyclic C(6)H(10) alkene (cyclohexene) were characterized by the use of a Fourier transform ion cyclotron mass spectrometer equipped with an electrospray
Carolina I Paris et al.
Journal of chemical ecology, 36(7), 689-698 (2010-06-16)
The emission of volatile organic compounds (VOCs) depends on temperature and light. Other factors such as insect herbivory also may modify VOC emission. In particular, aphid feeding promotes the release of new compounds and changes the composition of plant volatile
Hasan Yalçin et al.
Journal of medicinal food, 10(4), 715-719 (2007-12-27)
The chemical composition of the essential oil isolated from the leaves of the Laurus nobilis plant (from the Northern Cyprus Mountains) by hydrodistillation was analyzed by gas chromatography-mass spectrometry. Of the 81 compounds representing 98.74% of total oil, monocyclic monoterpenes
C Cabral et al.
Phytotherapy research : PTR, 26(9), 1352-1357 (2012-02-02)
Essential oils are known to possess antimicrobial activity against a wide spectrum of bacteria and fungi. In the present work the composition and the antifungal activity of the oils of Juniperus communis subsp. alpina (Suter) Čelak were evaluated. Moreover, the
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