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| Product | Description | |
|---|---|---|
| Juniper Berry Oil | Juniper Berry Oil. CAS No. 8002-68-4. FEMA No. 2604. Kosher: Y. VIGON Item # 501405. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Juniper Extract | Extract obtained from Juniperus Communis (Juniper) fruits. Contains 20% extract dissolved in water and glycerin. Has soothing, anti-irritant and calming properties. Uses: Creams, lotions and bath products. Group: Skin actives. CAS No. 7732-18-5 / 56-81-5 / 84603-69-0 / 122-99-6. Appearance: Light to medium amber liquid, characteristic odor. Catalog: CI-SC-0832. |  |
| Juniperus phoenicea wood extract | Use as antioxidant. Use as antibacterial agent. Group: Natural surfactants. Alternative Names: Juniper, Juniperus phoenicea, ext. CAS No. 90046-03-0. Catalog: ACM90046030. | |
| 16-Hydroxyhexadecanoic acid | 16-Hydroxyhexadecanoic acid (Juniperic acid) is an ester product. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Juniperic acid. CAS No. 506-13-8. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-W068212. |  |
| (1R, ?5S)?-2-?Hydroxy-?5-? (1-?methylethyl)?-bicyclo[3. 1. 0]?hexane-?2-?methanol | (1R, ?5S)?-2-?Hydroxy-?5-? (1-?methylethyl)?-bicyclo[3. 1. 0]?hexane-?2-?methanol is an intermediate in synthesizing (+)-Sabinene (S080750), a component of juniper berry oil having antibacterial and anti-fungal activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 1933700-48-1. Pack Sizes: 5mg, 10mg. Molecular Formula: C10H18O2. US Biological Life Sciences. |  Worldwide |
| (1R, 5S) -2- ( ( (t-Butyldiphenylsilyl) oxy) methyl) -5-isopropylbicyclo[3. 1. 0]hexan-2-ol | (1R, 5S) -2- ( ( (t-Butyldiphenylsilyl) oxy) methyl) -5-isopropylbicyclo[3. 1. 0]hexan-2-ol is an intermediate in synthesizing (+)-Sabinene (S080750), a component of juniper berry oil having antibacterial and anti-fungal activity. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg, 50mg. Molecular Formula: C26H36O2Si. US Biological Life Sciences. | Worldwide |
| (1R, 5S)-5-(1-Methylethyl)bicyclo[3. 1. 0]hexan-2-one | (1R, 5S)-5-(1-Methylethyl)bicyclo[3. 1. 0]hexan-2-one is an intermediate in synthesizing (+)-Sabinene (S080750), a component of juniper berry oil having antibacterial and antifungal activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 110716-99-9. Pack Sizes: 50mg, 100mg. Molecular Formula: C9H14O. US Biological Life Sciences. | Worldwide |
| acyl-CoA 5-desaturase | The enzyme, characterized from the plant Anemone leveillei, introduces a cis double bond at carbon 5 of acyl-CoAs that do not contain a double bond at position 8. In vivo it forms non-methylene-interrupted polyunsaturated fatty acids such as sciadonate and juniperonate. When expressed in Arabidopsis thaliana the enzyme could also act on unsaturated substrates such as palmitoyl-CoA. cf. EC 1.14.19.44, acyl-CoA (8-3)-desaturase. Group: Enzymes. Synonyms: acyl-CoA 5-desaturase (non-methylene-interrupted). Enzyme Commission Number: EC 1.14.19.37. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1001; acyl-CoA 5-desaturase; EC 1.14.19.37; acyl-CoA 5-desaturase (non-methylene-interrupted). Cat No: EXWM-1001. |  |
| Ferruginol | Botanical Source: Widely distributed in higher plants. Resin of Podocarpus ferrugineus. Also from Juniperus excelsa, Salvia mellifera, Taiwania cryptomerioides, Salvia hypargeia, Salvia lanigera, Salvia viridis, Cryptomeria japonica. Group: Biochemicals. Alternative Names: 3-Phenanthrenol, 4b,5,6,7,8,8a,9,10-octahydro-4b,8,8-trimethyl-2-(1-methylethyl)-, (4bS,8aS)-; Abieta-9(11),8(14),12-trien-12-ol; Abieta-8,11,13-triene-12-ol; (+)Ferruginol;(4bS, 8aS)-2-Isopropyl-4b, 8, 8-trimethyl-4b, 5, 6, 7, 8, 8a, 9, 10-octahydro-phenanthren-3-ol; Abieta-8,11,13-trien-12-ol. Grades: Plant Grade. CAS No. 514-62-5. Pack Sizes: 5mg. Molecular Formula: C20H30O, Molecular Weight: 286.45. US Biological Life Sciences. | Worldwide |
| Fomecin A | It is produced by the strain of Forme juniperinus. It has anti-gram positive bacterium, negative bacterium (weak), and mould (weak) activity, and it also has activity against flu virus PR-8. Human serum could reduce its activity. Synonyms: FOMECIN-A; Benzaldehyde, 2,3,4-trihydroxy-6-(hydroxymethyl)-; NSC 73231. Grades: 96%. CAS No. 1403-56-1. Molecular formula: C8H8O5. Mole weight: 184.15. |  |
| Kaempferia Galanga (Galanga Root Oil) - CO2 | Galangal CO2 select is extracted from the dried rhizomes (underground stems) of Kaempferia galanga, a small tropical plant that is closely related to ginger; it is commonly cultivated in India, Indonesia, and Malaysia for essential oilsproduction, medicinal use, and as an ingredient in curry. Galangal Root oil is fresh, spicy, woody, ginger-like oil, steam distilled from the plant's rhizome. In fact, Galangal Root is closely related to true ginger and cardamom so it's not surprising that Galangal Root blends well with these oils and shares similar notes. Blends Well With: Black Pepper, Cardamom, Carnation, Cedarwood, Chamomile (Roman), Cinnamon, Clove, Coriander, Cypress, Elemi, Fennel, Frankincense, Geranium, Ginger, Jasmine, Juniper Berry, Laurel Leaf, Lavandin, Lavender, Liquidambar (Styrax), Marjoram, Myrrh, Myrtle, Orris, Palmarosa, Patchouli, Pine, Rose, Sage, Sandalwood, Spikenard, Tarragon, Vetiver. Uses: Pharmaceutical. Group: Plant Extracts. INCI Names: Kaempferia Galanga Root Oil. Grades: INDUSTRIAL GRADE. CAS No. 92347-13-2. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: GL-001. Olfactive Profile: Fresh, spicy, characteristic odour of galanga. EC No: 296-200-2. Origin: Indonesia. |  New Jersey |
| (+)-Longifolene | Liquid. Alternative Names: D-longifolene; Junipen; Junipene; Kuromatsuen; Kuromatsuene; Longifolen; (+)-LONGIFOLENE, 98+%;C15 H24, 1,4-Methanoazulene, decahydro-4,8,8-trimethyl-9-methylene- [Longifolene:terpene]. CAS No. 475-20-7. Molecular formula: C15H24. Mole weight: 204.35. Appearance: Light-yellowish oil-shaped liquid. Purity: 0.75. IUPACName: (1R, 2S, 7S, 9S)-3, 3, 7-trimethyl-8-methylidenetricyclo[5.4.0.02, 9]undecane. Canonical SMILES: CC1(CCCC2(C3C1C(C2=C)CC3)C)C. Density: 0.928. ECNumber: 207-491-2. Catalog: ACM475207. | |
| (+)-Longifolene | Liquid. Group: Polymers. Alternative Names: D-longifolene; Junipen; Junipene; Kuromatsuen; Kuromatsuene; Longifolen; (+)-LONGIFOLENE, 98+%; C15 H24, 1,4-Methanoazulene, decahydro-4,8,8-trimethyl-9-methylene- [Longifolene:terpene]. CAS No. 475-20-7. Pack Sizes: 25 kg/DRUMS. Product ID: (1R, 2S, 7S, 9S)-3, 3, 7-trimethyl-8-methylidenetricyclo[5.4.0.02, 9]undecane. Molecular formula: 204.35. Mole weight: C15H24. CC1(CCCC2(C3C1C(C2=C)CC3)C)C. InChI=1S/C15H24/c1-10-11-6-7-12-13 (11)14 (2, 3)8-5-9-15 (10, 12)4/h11-13H, 1, 5-9H2, 2-4H3/t11-, 12-, 13+, 15-/m1/s1. PDSNLYSELAIEBU-GUIRCDHDSA-N. 75%. |  |
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