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00040590

α-Pinene

primary reference standard

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C10H16
Numero CAS:
Peso molecolare:
136.23
Numero CE:
Numero MDL:
Codice UNSPSC:
85151701
ID PubChem:
NACRES:
NA.24

Grado

primary reference standard

Livello qualitativo

Temp. autoaccensione

491 °F

Durata

limited shelf life, expiry date on the label

Produttore/marchio commerciale

HWI

Indice di rifrazione

n20/D 1.465 (lit.)

P. eboll.

155-156 °C (lit.)

Densità

0.858 g/mL at 25 °C (lit.)

Temperatura di conservazione

−20°C

Stringa SMILE

[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
GRWFGVWFFZKLTI-RKDXNWHRSA-N

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Categorie correlate

Descrizione generale

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

Applicazioni

Reference Standard in the analysis of herbal medicinal products

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

87.8 °F - closed cup

Punto d’infiammabilità (°C)

31 °C - closed cup


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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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