W285609
α-Phellandrene
≥75%, stabilized
Synonym(s):
2-Methyl-5-(1-methylethyl)-1,3-cyclohexadiene
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About This Item
Empirical Formula (Hill Notation):
C10H16
CAS Number:
Molecular Weight:
136.23
FEMA Number:
2856
EC Number:
Council of Europe no.:
2117
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
1.006
NACRES:
NA.21
Recommended Products
biological source
synthetic
Quality Level
grade
Halal
Kosher
reg. compliance
FDA 21 CFR 172.515
Assay
≥75%
optical activity
[α]20/D −139 to −110°, neat
contains
alpha-tocopherol as additive
refractive index
n20/D 1.474 (lit.)
density
0.85 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
Documentation
see Safety & Documentation for available documents
food allergen
no known allergens
Organoleptic
spicy; woody
SMILES string
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
InChI key
OGLDWXZKYODSOB-UHFFFAOYSA-N
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Related Categories
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).
Disclaimer
For R&D or non-EU Food use. Not for retail sale.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point(F)
116.6 °F - closed cup
Flash Point(C)
47 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
Kazuhiro Okamoto et al.
Organic letters, 10(19), 4387-4389 (2008-09-06)
Chiral dienes possessing the bicyclo[2.2.2]octadiene framework were prepared readily through the [4 + 2] cycloaddition of ( R)-alpha-phellandrene with methyl propiolate as the key step. Diene 9, substituted with a tertiary alcohol on one of the two double bonds, is
Christo S Sevov et al.
The Journal of organic chemistry, 73(20), 7909-7915 (2008-09-13)
Electron transfer catalysis is an effective method for the acceleration of Diels-Alder reactions between two substrates of similar electron density. The dependence of the selectivity of the Diels-Alder reaction between (R)-alpha-phellandrene and 4-methoxystyrene catalyzed by photoinduced electron transfer with tris(4-methoxyphenyl)
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
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