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00040590

α-Pinen

primary reference standard

Synonym(e):

(±)-2-Pinen, 2,6,6-Trimethylbicyclo[3.1.1]hept-2-en

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About This Item

Empirische Formel (Hill-System):
C10H16
CAS-Nummer:
80-56-8
Molekulargewicht:
136.23
EG-Nummer:
201-291-9
MDL-Nummer:
MFCD00001339
UNSPSC-Code:
85151701
PubChem Substanz-ID:
329746993
NACRES:
NA.24

Qualität

primary reference standard

Qualitätsniveau

300

Selbstzündungstemp.

491 °F

Haltbarkeit

limited shelf life, expiry date on the label

Hersteller/Markenname

HWI

Brechungsindex

n20/D 1.465 (lit.)

bp

155-156 °C (lit.)

Dichte

0.858 g/mL at 25 °C (lit.)

Lagertemp.

−20°C

SMILES String

[H][C@@]12CC=C(C)[C@@]([H])(C1)C2(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-/m1/s1

InChIKey

GRWFGVWFFZKLTI-RKDXNWHRSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

Produced and qualified by HWI pharma services GmbH.
Exact content by quantitative NMR can be found on the certificate.

Anwendung

Reference Standard in the analysis of herbal medicinal products

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

87.8 °F - closed cup

Flammpunkt (°C)

31 °C - closed cup

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
HWI03418
HWI00288-2
HWI00288-1
HWI00288-1

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(−)-α-Pinen 99%, optical purity ee: 97% (GLC)

Sigma-Aldrich

305715

(−)-α-Pinen

(−)-β-Pinen analytical standard

Supelco

80609

(−)-β-Pinen

(−)-α-Pinen 98%, optical purity ee: ≥81% (GLC)

Sigma-Aldrich

P45702

(−)-α-Pinen

Myrcen analytical standard

Supelco

64643

Myrcen

(+)-β-Pinen analytical standard

Supelco

80607

(+)-β-Pinen

(−)-β-Pinen ≥99%

Sigma-Aldrich

402753

(−)-β-Pinen

(R)-(+)-Limone primary reference standard

00590590

(R)-(+)-Limone

Mansour Znati et al.
Natural product communications, 7(7), 947-950 (2012-08-23)
The present work describes the chemical composition and evaluates the antimicrobial and the anti-acetylcholinesterase properties of the flower oil from the Tunisian Ferula lutea obtained by hydrodistillation and analyzed by combination of GC/FID and GC/MS. The chemical composition of the
Jeremy D Allison et al.
Environmental entomology, 41(6), 1587-1596 (2013-01-17)
In recent years, several attractant pheromones have been identified for cerambycid beetles, including 2-(undecyloxy)-ethanol (hereafter monochamol) for Monochamus galloprovincialis (Olivier), M. alternatus Hope, and M. scutellatus (Say). This study screened eight known cerambycid pheromones or their analogues (including monochamol) as
Ana Cristina Rivas da Silva et al.
Molecules (Basel, Switzerland), 17(6), 6305-6316 (2012-05-29)
The antimicrobial activities of the isomers and enantiomers of pinene were evaluated against bacterial and fungal cells. The agar diffusion test showed that only the positive enantiomers of the α- and β-isomers of pinene were active. The minimal inhibitory concentration
Li Qi et al.
Journal of the Air & Waste Management Association (1995), 62(12), 1359-1369 (2013-02-01)
This work investigates the oxidative aging of preformed secondary organic aerosol (SOA) derived from alpha-pinene ozonolysis (-100 ppb(v) hydrocarbon [HC(x)] with excess of O3) within the University of California-Riverside Center for Environmental Research and Technology environmental chamber that occurs after
Anthony Montenegro et al.
The journal of physical chemistry. A, 116(49), 12096-12103 (2012-11-10)
The kinetics of reactions of α-pinene and β-pinene with hydroxyl radicals (OH) has been investigated at 1-8 Torr and 240-340 K using the relative rate/discharge flow/mass spectrometry (RR/DF/MS) technique. Our kinetic results indicate that at 298 K the rate constant
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