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| Product | Description | |
|---|---|---|
| Bay Laurel Extract | Extract obtained from Laurus Nobilis (Bay Laurel) leaves. Contains 20% extract dissolved in water and glycerin. Has aromatic, anti-dandruff, astringent and soothing properties. Uses: Hair, bath, and topical skin preparations. Group: Skin actives. CAS No. 7732-18-5 / 56-81-5 / 84603-73-6 / 122-99-6. Appearance: Light to medium amber liquid, herbal odor. Catalog: CI-SC-0833. |  |
| Camphor | Camphor is found in the wood of the camphor laurel (Cinnamomum camphora), a large evergreen tree found in East Asia. It can be used as a repellent, a plasticizer for nitrocellulose, a moth repellent, and an antimicrobial substance. Uses: Anti-infective agents, local. Synonyms: Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-; (±)-Camphor; 1,7,7-Trimethylbicyclo[2.2.1]-2-heptanone; 1,7,7-Trimethylnorcamphor; 2-Bornanone; 2-Camphanone; DL-Camphor; Alphanon; Borneo camphor; dl-Camphor; HCXL 8899; MeSH ID: D002164; Racemic camphor; Root bark oil; Spirit of camphor. Grades: ≥95%. CAS No. 76-22-2. Molecular formula: C10H16O. Mole weight: 152.23. |  |
| Camphor | Kampfer is a waxy, flammable, white, or transparent solid with a strong aroma. It is a terpenoid with the chemical formula C10H16O. It is found in the wood of the Kampfer laurel (Cinnamomum camphora), a large evergreen tree found in Asia (particularly in Sumatra, Indonesia, and Borneo), and also of the unrelated Kapur tree, a tall timber tree from the same region. It also occurs in some other related trees in the laurel family, notably Ocotea usambarensis. The oil in rosemary leaves (Rosmarinus officinalis), in the mint family, contains 10 to 20%, Kampfer, while camphorweed (Heterotheca) only contains some 5%. Camphor can also be synthetically produced from the oil of turpentine. It is used for its scent, as an ingredient in cooking (mainly in India), as an embalming fluid, for medicinal purposes, and in religious ceremonies. A major source of camphor in Asia is camphor basil (the parent of African blue basil).The molecule has two possible enantiomers is shown in the structural diagrams. The structure on the left is the naturally occurring (R)-form, while its mirror image shown on the right is the (S)-form.Norcamphor is a Kampfer derivative with the three methyl groups replaced by hydrogen. Group: Inhibitors. Alternative Names: 1,7,7-Trimethyl-bicyclo[2.2.1]heptan-2-on. CAS No. 76-22-2. Molecular formula: C10H16O. Mole weight: 152.23. Appearance: Powder. Purity: 0.98. IUPACName: 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one. Canonica | |
| Cinnamon Extract | Cinnamon extract is prepared from the dry bark of the cinnamon (cinnamomum) lauraceae plants, which latin name is cinnamomum cassia presl. Cinnamomum is a genus of evergreen aromatic trees and shrubs belonging to the laurel family, lauraceae. The species of cinnamomum have aromatic oils in their leaves and bark. Cinnamon polyphenols and flavonoids is the major ingredients found in cinnamon bark extract. Cinnamon extract is commonly used for kidney impotence, tonifying yang, and promoting blood circulation, cold-dispelling and relieve pain. Group: Others. Cinnamon Extract; cinnamomum cassia presl. Cat No: EXTC-002. |  |
| 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 |
| Norisoboldine | Norisoboldine. Group: Biochemicals. Alternative Names: Laurelliptine. Grades: Plant Grade. CAS No. 23599-69-1. Pack Sizes: 20mg. Molecular Formula: C18H19NO4, Molecular Weight: 313.348. US Biological Life Sciences. |  Worldwide |
| Norisoboldine | Norisoboldine might be a potential therapeutic agent for rheumatoid arthritis, and it functions through protecting joint destruction as well as regulating the abnormal immune responses. Synonyms: norisoboldine; (+)-Laurelliptine; (+)-N-Norisoboldine; (6aS)-5,6,6a,7-Tetrahydro-2,10-dimethoxy-4H-dibenzo[de,g]quinoline-1,9-diol; (S)-(+)-Laurelliptine. Grades: >98%. CAS No. 23599-69-1. Molecular formula: C18H19NO4. Mole weight: 313.35. | |
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