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W285609

Sigma-Aldrich

α-Phellandrene

≥75%, stabilized

Synonyme(s) :

2-Methyl-5-(1-methylethyl)-1,3-cyclohexadiene

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About This Item

Formule empirique (notation de Hill):
C10H16
Numéro CAS:
99-83-2
Poids moléculaire :
136.23
Numéro FEMA:
2856
Numéro CE :
202-792-5
Conseil de l'Europe Nº :
2117
Numéro MDL:
MFCD00040419
Code UNSPSC :
12164502
ID de substance PubChem :
24901345
Numéro Flavis :
1.006
Nomenclature NACRES :
NA.21

Source biologique

synthetic

Niveau de qualité

400

Qualité

Halal
Kosher

Conformité réglementaire

FDA 21 CFR 172.515

Pureté

≥75%

Activité optique

[α]20/D −139 to −110°, neat

Contient

alpha-tocopherol as additive

Indice de réfraction

n20/D 1.474 (lit.)

Densité

0.85 g/mL at 25 °C (lit.)

Application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

Allergène alimentaire

no known allergens

Propriétés organoleptiques

spicy; woody

Chaîne SMILES 

CC(C)C1CC=C(C)C=C1

InChI

1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4-6,8,10H,7H2,1-3H3

Clé InChI

OGLDWXZKYODSOB-UHFFFAOYSA-N

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Catégories apparentées

Application


  • Does green mean clean Volatile organic emissions from regular versus green cleaning products.: This research compares the volatile organic compound (VOC) emissions from conventional and green cleaning products, identifying a-phellandrene as a common component. The findings highlight the environmental impact of green products and their effectiveness (Harding-Smith et al., 2024).

  • RNA-Seq-Based Transcriptomics and GC-MS Quantitative Analysis Reveal Antifungal Mechanisms of Essential Oil of Clausena lansium (Lour.) Skeels Seeds against Candida albicans.: The study uses RNA-Seq and GC-MS to investigate the antifungal properties of Clausena lansium essential oil, which contains a-phellandrene, against Candida albicans, providing insights into its potential therapeutic applications (Ma et al., 2023).

  • Unveiling the Anti-Cholera and Active Diabetic Renoprotective Compounds of Maqian Essential Oil: A Computational and Molecular Dynamics Study.: This study identifies a-phellandrene as an active compound in Maqian essential oil with anti-cholera and renoprotective effects, suggesting its potential for treating cholera and protecting against diabetic renal damage (Dahab et al., 2023).

  • Electrophysiological and Behavioral Responses of Batocera horsfieldi Hope to Volatiles from Pistacia chinensis Bunge.: This research examines the responses of Batocera horsfieldi to volatiles, including a-phellandrene, from Pistacia chinensis. The findings have implications for pest management strategies using natural volatiles (Fan et al., 2023).

Clause de non-responsabilité

For R&D or non-EU Food use. Not for retail sale.

Pictogrammes

FlameHealth hazard
GHS02,GHS08

Mention d'avertissement

Danger

Mentions de danger

H226,H304

Classification des risques

Asp. Tox. 1 - Flam. Liq. 3

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

116.6 °F - closed cup

Point d'éclair (°C)

47 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Sigma-Aldrich

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α-Terpinene analytical standard

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Huai-sheng Hu et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 32(1), 67-70 (2009-05-19)
The chemical constituents and antimicrobial activity of the essential oil from Acanthopanax brachypus were studied. The essential oil was extracted from the stem of A. brachypus by steam distillation, and its antimicrobial activity was tested in vitro. The chemical constituents
Gökalp İşcan et al.
Chemistry & biodiversity, 9(8), 1525-1532 (2012-08-18)
Terpene derivatives converted by microbial biotransformation constitute an important resource for natural pharmaceutical, fragrance, and aroma substances. In the present study, the monoterpene α-phellandrene was biotransformed by 16 different strains of microorganisms (bacteria, fungi, and yeasts). The transformation metabolites were
M Miyazawa et al.
Journal of agricultural and food chemistry, 48(7), 2893-2895 (2000-07-18)
gamma-Terpinene was mixed in artificial diet at a concentration of 1 mg/g of diet, and the diet was fed to the last instar larvae of common cutworm (Spodoptera litura). Metabolites were recovered from frass and analyzed spectroscopically. gamma-Terpinene was transformed
David F Lima et al.
The Journal of pharmacy and pharmacology, 64(2), 283-292 (2012-01-10)
The aim of this work was to investigate the antinociceptive property of α-phellandrene (α-PHE) in experimental nociception models and possible mechanisms involved. Mass spectrometry was used to evaluate the purity and molecular mass of α-PHE. Macrophages from mice peritoneal cavity
S Foss et al.
Systematic and applied microbiology, 21(2), 237-244 (1998-08-15)
Four pseudomonad strains 51Men, 54Pin, 62Car and 65Phen were recently isolated on the monoterpenes (+)-menthene, alpha-pinene, 2-carene and alpha-phellandrene as sole carbon source and nitrate as electron acceptor. These bacteria were characterised. The motile, mesophilic, Gram-negative rods had a strictly
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