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| Product | Description | |
|---|---|---|
| Carene Delta-3 Natural | Carene Delta-3 Natural. CAS No. 13466-78-9. FEMA No. 3821. Kosher: Y. VIGON Item # 503554. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essetial Oils. |  America & Internationally |
| (1S)-(+)-3-Carene | (1S)-(+)-3-Carene is used in the synthesis of compounds with various odoriferous properties. It is used by the perfume and fragrance industry or in perfume materials preparation. Group: Biochemicals. Grades: Highly Purified. CAS No. 498-15-7. Pack Sizes: 100mg, 250mg. Molecular Formula: C10H16, Molecular Weight: 136.229999999999. US Biological Life Sciences. |  Worldwide |
| (1S)-(+)-3-Carene | (1S)-(+)-3-Carene. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (1S,6R)-3-Carene. Product Category: Heterocyclic Organic Compound. Appearance: Clear very slightly yellow liquid. CAS No. 498-15-7. Molecular formula: C10H16. Mole weight: 136.23. Purity: 0.98. IUPACName: (1S,6R)-3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene. Canonical SMILES: CC1=CCC2C(C1)C2(C)C. Density: 0.865 g/mL at 25 °C(lit.). Product ID: ACM498157. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 3-Carene | 3-Carene is a bicyclic monoterpene in essential oils extracted from pine trees. 3-Carene inhibits nociceptive stimulus-induced inflammatory infiltrates and COX-2 overexpression, and with antinociceptive effect. 3-Carene stimulates the activity and expression of alkaline phosphatase that is an early phase marker of osteoblastic differentiation [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 13466-78-9. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-N6663. |  |
| 3-Carene | 3-Carene is a mutagenic compound that may be found in the fumes of heating freshly cut spruce and birch chips. 3-Carene is also found i many esential oils and it inhibits acetylcholinesterase activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 13466-78-9. Pack Sizes: 100g, 250g. Molecular Formula: C10H16. US Biological Life Sciences. | Worldwide |
| 3-Carene-D3 | Deuterium labelled isotope of 3-Carene, which is a mutagenic compound that may be found in the fumes of heating freshly cut spruce and birch chips. 3-Carene is also found i many esential oils and it inhibits acetylcholinesterase activity. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C10H13D3, Molecular Weight: 139.25. US Biological Life Sciences. | Worldwide |
| 4-Acetyl carene | 4-Acetyl carene. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4-ACETYL CARENE;CARENKO;1-(4,7,7-trimethylbicyclo[4.1.0]hept-4-en-3-yl)-ethanon;1-[4,7,7-trimethylbicyclo[4.1.0]hept-4-en-3-yl]-Ethanone;car-2-en-4-ylmethylketone;4-acetyl-3,7,7-trimethylbicyclo(4.1.0)hept-2-ene;Ethanone, 1-(4,7,7-trimethylbicyclo4.1.0he. Product Category: Heterocyclic Organic Compound. CAS No. 3608-11-5. Molecular formula: C12H18O. Mole weight: 178.27. Product ID: ACM3608115. Alfa Chemistry ISO 9001:2015 Certified. Categories: Acetylcarene. | |
| (-)-β-pinene synthase | Cyclase II of Salvia officinalis (sage) produces about equal parts (-)-α-pinene, (-)-β-pinene and (-)-camphene, plus traces of other monoterpenoids. The enzyme, which requires Mg2+ (preferred to Mn2+), can also use (3S)-Linalyl diphosphate (preferred to (3R)-linalyl diphosphate). The enzyme from Abies grandis (grand fir) produces roughly equal parts of (-)-α-pinene and (-)-β-pinene. Cyclase IV from Pinus contorta (lodgepole pine) produces 63% (-)-β-pinene, 26% 3-carene, and traces of α-pinene. Synthase III from Pinus taeda (loblolly pine) forms (-)-β-pinene with traces of α-pinene and requires Mn2+ and K+ (Mg2+ is ineffective). A clone...a spruce) forms 30% (-)-β-pinene and 70% (-)-α-pinene. See also EC 4.2.3.119, (-)-α-pinene synthase, EC 4.2.3.117, (-)-camphene synthase, and EC 4.2.3.107 (+)-3-carene synthase. Group: Enzymes. Synonyms: β-geraniolene synthase; (-)-(1S,5S)-pinene synthase; geranyldiphosphate diphosphate lyase (pinene forming). Enzyme Commission Number: EC 4.2.3.120. 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-5133; (-)-β-pinene synthase; EC 4.2.3.120; β-geraniolene synthase; (-)-(1S,5S)-pinene synthase; geranyldiphosphate diphosphate lyase (pinene forming). Cat No: EXWM-5133. |  |
| (+)-car-3-ene synthase | The enzyme reacts with (3S)-linalyl diphosphate twice as rapidly as geranyl diphosphate, but 25 times as rapidly as (3R)-linalyl diphosphate. It is assumed that (3S)-linalyl diphosphate is normally formed as an enzyme bound intermediate in the reaction. In the reaction the 5-pro-R hydrogen of geranyl diphosphate is eliminated during cyclopropane ring formation. In Picea abies (Norway spruce) and Picea sitchensis (Sitka spruce) terpinolene is also formed. See EC 4.2.3.113 terpinolene synthase. (+)-Car-3-ene is associated with resistance of Picea sitchensis (Sitka spruce) to white pine weevil. Group: Enzymes. Synonyms: 3-carene cyclase; 3-carene synthase; 3CAR; (+)-3-carene synthase. Enzyme Commission Number: EC 4.2.3.107. 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-5118; (+)-car-3-ene synthase; EC 4.2.3.107; 3-carene cyclase; 3-carene synthase; 3CAR; (+)-3-carene synthase. Cat No: EXWM-5118. | |
| ipsdienol synthase | A cytochrome P-450 heme-thiolate protein. Involved in the insect aggregation pheromone production. Isolated from the pine engraver beetle, Ips pini. A small amount of (S)-ipsdienol is also formed. In vitro it also hydroxylated (+)- and (-)-α-pinene, 3-carene, and (+)-limonene, but not α-phellandrene, (-)-β-pinene, γ-terpinene, or terpinolene. Group: Enzymes. Synonyms: myrcene hydroxylase; CYP9T2; CYP9T3. Enzyme Commission Number: EC 1.14.14.31. 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-0929; ipsdienol synthase; EC 1.14.14.31; myrcene hydroxylase; CYP9T2; CYP9T3. Cat No: EXWM-0929. | |
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