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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:
80-56-8
Peso molecolare:
136.23
Numero CE:
201-291-9
Numero MDL:
MFCD00001339
Codice UNSPSC:
85151701
ID PubChem:
329746993
NACRES:
NA.24

Grado

primary reference standard

Livello qualitativo

300

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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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

H226,H304,H315,H317,H410

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

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
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

Myrcene analytical standard

Supelco

64643

Myrcene

(+)-β-Pinene analytical standard

Supelco

80607

(+)-β-Pinene

(−)-β-Pinene ≥99%

Sigma-Aldrich

402753

(−)-β-Pinene

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

00590590

(R)-(+)-Limonene

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
Anton Miró et al.
BMC bioinformatics, 13, 90-90 (2012-05-12)
The estimation of parameter values for mathematical models of biological systems is an optimization problem that is particularly challenging due to the nonlinearities involved. One major difficulty is the existence of multiple minima in which standard optimization methods may fall
Kaytlin M Henry et al.
Environmental science & technology, 46(22), 12347-12354 (2012-10-24)
Secondary organic aerosol formation from volatile precursors can be thought of as a succession of generations of reaction products. Here, we constrain first-generation SOA formation from the α-pinene + OH reaction and also study SOA formation from α-pinene ozonolysis carried
Lindsay Renbaum-Wolff et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(20), 8014-8019 (2013-04-27)
Particles composed of secondary organic material (SOM) are abundant in the lower troposphere. The viscosity of these particles is a fundamental property that is presently poorly quantified yet required for accurate modeling of their formation, growth, evaporation, and environmental impacts.
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
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