- α-phellandrene
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- $1.00 / 1kg
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2024-04-15
- CAS:99-83-2
- Min. Order: 1kg
- Purity: 99.9%
- Supply Ability: 10 ton/month
- ALPHA-PHELLANDRENE
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- $100.00 / 25kg
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2024-01-04
- CAS:99-83-2
- Min. Order: 25kg
- Purity: 99%
- Supply Ability: 2000kgs
- ALPHA-PHELLANDRENE
-
- $0.00 / 25KG
-
2023-10-24
- CAS:99-83-2
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 50000KG/month
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| | ALPHA-PHELLANDRENE Basic information |
| Product Name: | ALPHA-PHELLANDRENE | | Synonyms: | 1-ISOPROPYL-4-METHYL-2,4-CYCLOHEXADIENE;ALPHA-PHELLANDRENE;5-ISOPROPYL-2-METHYL-1,3-CYCLOHEXADIENE;ALPHA-PHELLANDRENE FCC;P-MENTHA-1,5-DIENE 70%;α-phellandrene,R-(-)-1,5-menthadiene,2-methyl-5-isopropyl-1,3-cyclohexadiene,α-phellandrene;1-ISOPROPYL-4-METHYL-2,4-CYCLOHEXADIENE,70%;D-ALPHA-PHELLANDRENE | | CAS: | 99-83-2 | | MF: | C10H16 | | MW: | 136.23 | | EINECS: | 202-792-5 | | Product Categories: | Alphabetical Listings;Flavors and Fragrances;O-P | | Mol File: | 99-83-2.mol |  |
| | ALPHA-PHELLANDRENE Chemical Properties |
| Boiling point | 185.55°C (rough estimate) | | density | 0.85 g/mL at 25 °C(lit.) | | refractive index | n20/D 1.474(lit.) | | FEMA | 2856 | ALPHA-PHELLANDRENE | | Fp | 117 °F | | storage temp. | Store below +30°C. | | solubility | Benzene: Soluble; Chloroform: Soluble | | form | An oil | | Melting point | <25 °C | | Odor | at 10.00 % in dipropylene glycol. citrus herbal terpene green woody peppery | | Odor Type | terpenic | | optical activity | [α]20/D 139 to 110°, neat | | JECFA Number | 1328 | | Merck | 13,7277 | | Stability: | Light Sensitive, Temperature Sensitive | | LogP | 4.43 | | CAS DataBase Reference | 99-83-2(CAS DataBase Reference) | | EPA Substance Registry System | 1,3-Cyclohexadiene, 2-methyl-5-(1-methylethyl)- (99-83-2) |
| | ALPHA-PHELLANDRENE Usage And Synthesis |
| Chemical Properties | α-Phellandrene has a pleasant, fresh, citrus, peppery odor with a discrete mint note. This compound is also reported as
having a minty, herbaceous odor. | | Occurrence | The d-form has been reported found in the essential oils of bitter fennel, Ceylon cinnamon leaves, star anise,
Curcuma longa and other essential oils; the l-form has been reported found in various eucalyptus oils, orange peel oil, angelica,
Lantana camara and other oils. Reported found in over 100 foods and beverages including apricot, many citrus peel oils and juices,
black currants, papaya, raspberry, strawberry, carrot, celery leaves and seed, bell pepper, tomato, cinnamon, cumin seed, ginger,
Mentha oils, nutmeg, pepper, mace, parsley, thyme, Gruyere cheese, cured pork, hop oil, beer, tea, pecan, passion fruit, sweet and
wild marjoram, mango, parsnip, cardamom, coriander seed, gin, litchi, dill herb and seed, lovage leaf and seed, caraway, juniper
berry, laurel, bitter and sweet fennel, myrtle leaf and berry, sage, nectarine, pimento leaf and berry and mastic gum leaf oil. | | Uses | α-Phellandrene is an essential oil component, found to have bactericidal activity. | | Definition | ChEBI: One of a pair of phellandrene cyclic monoterpene double-bond isomers in which both double bonds are endocyclic (cf. alpha-phellandrene, where one of them is exocyclic). | | Aroma threshold values | Detection: 40 to 200 ppb | | Taste threshold values | Taste characteristics at 20 ppm: terpenic, citrus-lime with a fresh green note. | | General Description | α-Phellandrene is monoterpene reported to be one of the aroma compounds of black (Piper nigrum) and white ‘‘Ashanti pepper′′ (Piper guineense). It also occurs in the leaves of basil. | | Safety Profile | Mdly toxic by
ingestion. A severe human skin irritant.
Incompatible with air. Flammable liquid
when exposed to heat, sparks, or flame.
When heated to decomposition it emits
acrid smoke and irritating fumes. | | Synthesis | The l-form by isolation from Eucalyptus numerosa and similar oils; also from the manufacture of synthetic menthol. |
| | ALPHA-PHELLANDRENE Preparation Products And Raw materials |
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