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00040590

α-Pinene

primary reference standard

Synonyme(s) :

(±)-2-Pinene, 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene

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About This Item

Formule empirique (notation de Hill):
C10H16
Numéro CAS:
80-56-8
Poids moléculaire :
136.23
Numéro CE :
201-291-9
Numéro MDL:
MFCD00001339
Code UNSPSC :
85151701
ID de substance PubChem :
329746993
Nomenclature NACRES :
NA.24

Qualité

primary reference standard

Niveau de qualité

300

Température d'inflammation spontanée

491 °F

Durée de conservation

limited shelf life, expiry date on the label

Fabricant/nom de marque

HWI

Indice de réfraction

n20/D 1.465 (lit.)

Point d'ébullition

155-156 °C (lit.)

Densité

0.858 g/mL at 25 °C (lit.)

Température de stockage

−20°C

Chaîne SMILES 

[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

Clé InChI

GRWFGVWFFZKLTI-RKDXNWHRSA-N

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Catégories apparentées

Description générale

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

Application

Reference Standard in the analysis of herbal medicinal products

Mention d'avertissement

Danger

Mentions de danger

H226,H304,H315,H317,H410

Classification des risques

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

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

87.8 °F - closed cup

Point d'éclair (°C)

31 °C - closed cup

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Certificats d'analyse (COA)

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

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

Sigma-Aldrich

305715

(−)-α-Pinene

(−)-β-Pinene analytical standard

Supelco

80609

(−)-β-Pinene

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

Sigma-Aldrich

P45702

(−)-α-Pinene

Myrcène analytical standard

Supelco

64643

Myrcène

(+)-β-Pinene analytical standard

Supelco

80607

(+)-β-Pinene

(−)-β-Pinene ≥99%

Sigma-Aldrich

402753

(−)-β-Pinene

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

00590590

(R)-(+)-Limonène

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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