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| Product | Description | |
|---|---|---|
| Ethyl Acetate Natural | Ethyl Acetate Natural. CAS No. 141-78-6. FEMA No. 2414. Kosher: Y. VIGON Item # 500126. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essetial Oils. |  America & Internationally |
| Dimethyl Sulfide Natural 5% in Ethyl Acetate Natural | Dimethyl Sulfide Natural 5% in Ethyl Acetate Natural. CAS No. MIXTURE. Kosher: Y. VIGON Item # 507630. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Ethyl Aceto Acetate Natural | Ethyl Aceto Acetate Natural. CAS No. 141-97-9. FEMA No. 2415. Kosher: Y. VIGON Item # 504423. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essetial Oils. | America & Internationally |
| Ethyl Phenyl Acetate Natural | Ethyl Phenyl Acetate Natural. CAS No. 101-97-3. FEMA No. 2452. Kosher: Y. VIGON Item # 504744. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essetial Oils. | America & Internationally |
| Phenyl Ethyl Acetate Natural | Phenyl Ethyl Acetate Natural. CAS No. 103-45-7. FEMA No. 2857. Kosher: Y. VIGON Item # 503699. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essetial Oils. | America & Internationally |
| Ajoene | Ajoene, a garlic-derived compound, is an antithrombotic and antifungal agent. Ajoene inhibits proliferation and induces apoptosis of human leukaemia CD34-negative cells including HL-60, U937, HEL and OCIM-I. Anticancer activities [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 92285-01-3. Pack Sizes: 1 mg (21.33 mM * 200 μL in Ethyl acetate). Product ID: HY-106784. |  |
| Chloramphenicol acetate | It is a naturally-occurring co-metabolite of chloramphenicol in streptomyces venezuelae with albeit significantly lower potency. It is the major product of chloramphenicol acetyltransferase. Synonyms: 3-O-Acetylchloramphenicol; Chloramphenicol 3-acetate; 3-Acetylchloramphenicol; Acetamide, N-(1-((acetyloxy)methyl)-2-hydroxy-2-(4-nitrophenyl)ethyl)-2,2-dichloro-, (R-(R*,R*))-; D-threo-(-)-2,2-Dichloro-N-[β-hydroxy-α-(hydroxymethyl)-p-nitrophenethyl]acetamide α-Acetate. Grades: >99% by HPLC. CAS No. 10318-16-8. Molecular formula: C13H14Cl2N2O6. Mole weight: 365.17. |  |
| Ethyl lactate,C5H10O3,97-64-3 | Ethyl Lactate is a solvent manufactured from l(+) lactic acid which is miscible in water and most organic solvents and is cleared for use as a flavoring agent. it is a naturally occurring constituent of california and spanish sherries. it is a clear, colorless, nontoxic liquid of low volatility, having a ph of 7-7.5. it is used as a food and beverage flavoring agent.formulationsand recently as a co-solvent in emulsions and microemulsion technologies. It has also been used as a solvent for nitrocellulose, cellulose acetate, cellulose ethers, polyvinyl and other resins. It has been applied topically in the treatment of acne vulgaris,where it accumulates in the sebaceous glands and is hydrolyzed to ethanol and lactic acid, lowering the skin pH and exerting a bactericidal effect. Group: Platinum catalysts. Alternative Names: ethyl-lactate; Ethyl racemic-lactate; I14-2597; Ethyl 2-hydroxypropanoate; Mono-Ethyl mono-lactate; Tox21_200889; SY030456; Lactic acid, ethyl ester; L0003; Propanoicacid, 2-hydroxy-, ethyl ester, (2R)-. CAS No. 97-64-3. Molecular formula: C5H10O3. Mole weight: 118.132g/mol. IUPACName: ethyl 2-hydroxypropanoate. Canonical SMILES: CCOC(=O)C(C)O. Density: 1.03 at 68 ° F (USCG, 1999);1.0328 g.cu cm at 20 deg C;1.03. ECNumber: 202-598-0. Catalog: ACM97643. |  |
| Jesaconitine | Jesaconitine is a natural compound that has been shown to have anti-inflammatory properties. It has been shown to inhibit the activity of cyclooxygenase and lipoxygenase enzymes, which are involved in the production of prostaglandins. Jesaconitine also inhibits the expression of nuclear DNA and suppresses myeloma cells by inhibiting their ability to synthesize proteins. Jesaconitine has also been shown to inhibit chronic arthritis in animal models by suppressing inflammation and preventing joint damage. This compound is not active against nonsteroidal anti-inflammatory drugs such as ibuprofen, diclofenac, and naproxen. Jesaconitine can be extracted from the plant Angelica Dahurica or synthesized in laboratories. It is soluble in trifluoroacetic acid (TFA) and can be analyzed using nuclear magnetic resonance spectroscopy with high values for matrix effect and control analysis. Group: Other alkaloids. Alternative Names: Diesaconitine(1a,3a,6a,14a,15a,16b)-20-Ethyl-1,6,16-triMethoxy-4-(MethoxyMethyl)-aconitane-3,8,13,14,15-pentol 8-Acetate 14-(4-Meth oxybenzoate). CAS No. 16298-90-1. Molecular formula: C35H49NO12. Mole weight: 675.76 g/mol. Canonical SMILES: CCN1C[C@@]2 ([C@@H] (C[C@@H] ([C@@]34[C@@H]2[C@H] ([C@@H] ([C@H]31)[C@@]5 ([C@@H]6[C@H]4C[C@@] ([C@@H]6OC (=O)C7=CC=C (C=C7)OC) ([C@H] ([C@@H]5O)OC)O)OC (=O)C)OC)OC)O)COC. Catalog: ACM16298901. | |
| Severine palmitate | Severine is a natural product that is extracted from the leaves of Rutaceae. It has been shown to have anticancer properties against cholangiocarcinoma cells, which may be due to its ability to inhibit the proliferation and induce apoptosis in these cells. Severine is converted into severine palmitate by acetylation, forming a new molecule with antiproliferative activity. The chemical structure of severine palmitate consists of an apigenin-derived crenulata skeleton with a natural product flavone at C-6 and a diacetate ester at C-7. Severine palmitate has been shown to be effective against human cholangiocarcinoma cell lines in vitro, as well as in vivo when administered orally or intravenously. Group: Other alkaloids. Alternative Names: O-Palmitoylseverine4- [4- [2- (Benzoylamino) ethyl] phenoxy] - 1- [(3, 3- dimethyloxiranyl) methyl] - 2- methyl- 2- butenyl ester h exadecanoic acid. CAS No. 74493-88-2. Molecular formula: C41H61NO5. Mole weight: 647.93 g/mol. Catalog: ACM74493882. | |
| (1R,2S,5R)-(-)-Menthol 2,3,4-Tri-O-acetyl- β-D-glucuronide Methyl Ester | (1R,2S,5R)-(-)-Menthol β-D-Glucuronide (M218880) derivative, a metabolite of L-(-)-Menthol (M218875), the natural form of Methanol. Group: Biochemicals. Alternative Names: (1R, 2S, 5R) -5-Methyl-2- (1-methylethyl) cyclohexyl2, 3, 4-Tri-O-acetyl- β-D-glucuronide Methyl Ester; l-Menthyl 2,3,4-Tri-O-acetyl- β-D-glucuronide Methyl Ester; [1R-(1α,2 β,5 β)]-5-?ethyl-2-(1-methylethyl)cyclohexyl 2,3,4-Tri-O-acetyl- β-D-glucuronide Methyl Ester. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences. |  Worldwide |
| 2-Acetyl-3-ethylpyrazine | 2-Acetyl-3-ethylpyrazine is an endogenous metabolite. Uses: Scientific research. Group: Natural products. CAS No. 32974-92-8. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-W039157. | |
| Acetyl-2 Pyrazine Natural 5% in Ethyl Alcohol | Acetyl-2 Pyrazine Natural 5% in Ethyl Alcohol. CAS No. MIXTURE. Kosher: Y. VIGON Item # 508399. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essential Oils. | America & Internationally |
| Melatonin | Melatonin is an indoleamine that has traditionally been considered only a sleep hormone in humans. Recently it has been found to naturally occur in plants and has shown attributes which could categorize it as an auxin. It has roles in in plant defense, and stress. Uses: Initially discovered in animals and later found in a majority of plant species, indoleamine neurotransmitter melatonin is a multifunctional signaling molecule. some of these functions include roles in plant defense, growth, development, responses to stress, antioxidant activity, and many more evidence indicates melatonin and serotonin have a relationship similar to how the interaction of cytokinin and auxin affect plant growth. Group: Inhibitors. Alternative Names: N-Acetyl-5-methoxytryptamine. CAS No. 73-31-4. Molecular formula: C13H16N2O2. Mole weight: 232.28 g/mol. Appearance: White powder. Purity: 98%+. IUPACName: N-[2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide. Canonical SMILES: CC(=O)NCCC1=CNC2=C1C=C(C=C2)OC. Density: 1.175 g/cm³. ECNumber: 200-797-7. Catalog: ACM73314. | |
| MWNTs ethyl acetate suspension | Carbon black oil appears as a dark colored liquid with a petroleum-like odor. Less dense than water and insoluble in water. Vapors heavier than air.;Carbon, activated is a black grains that have been treated to improve absorptive ability. May heat spontaneously if not properly cooled after manufacture.;Carbon, animal or vegetable origin appears as a black powder or granular mixed with a tar or starch and water binder pressed into regular lumps or briquettes. Heats slowly and ignites in air especially if wet.;Graphite (natural) appears as a mineral form of the element carbon. Hexagonal crystals or thin leaf-like layers. Steel-gray to black with a metallic luster and a greasy feel. An electrical conductor. Used for high-temperature crucibles, as a lubricant and in "lead" pencils.;DryPowder; DryPowder, Liquid; DryPowder, PelletsLargeCrystals; DryPowder, PelletsLargeCrystals, WetSolid, OtherSolid, Liquid; DryPowder, WetSolid, Liquid; Liquid; OtherSolid; OtherSolid, GasVapor, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid, Liquid; WetSolid; WetSolid, Liquid;OtherSolid; PelletsLargeCrystals;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetSolid;DryPowder; DryPowder, OtherSolid; DryPowder, PelletsLargeCrystals; DryPowder, WetSolid; Liquid; OtherSolid; PelletsLargeCrystals; PelletsLargeCrystals, OtherSolid; WetS |  |
| Vinblastine | Vinblastine, an inhibitor of nAChR, is a natural alkaloid isolated from the plant Vinca rosea Linn. It binds to tubulin and inhibits microtubule formation, leading to disruption of mitotic spindle assembly and arrest of tumor cells in the M-phase of the cell cycle. It may also interfere with the metabolism of amino acids, cyclic AMP, and glutathione. It is used to treat malignant lymphoma. Uses: Antitumor. Synonyms: [3aR-[3aa, 4b, 5b, 5ab, 9(3R*, 5S*, 7R*, 9S*), 10bR*, 13aa]]-Methyl 4-(acetyloxy)-3a-ethyl-9-[5-ethyl-1,4,5,6,7,8,9,10-octahydro-5-hydroxy-9-(methoxycarbonyl)-2H-3,7-methanoazacycloundecino[5,4-b]indol-9-yl]-3a,4,5,5a,6,11,12,13a-octahydro-5-hydroxy-8-methoxy-6-methyl-1H-indolizino[8,1-cd]carbazole-5-carboxylate; 1H-Indolizino[8,1-cd]carbazole, vincaleukoblastine deriv.; 1H-Indolizino(8,1-cd)carbazole-5-carboxylic acid, 4-(acetyloxy)-3a-ethyl-9-(5-ethyl-1,4,5,6,7,8,9,10-octahydro-5-hydroxy-9-(methoxycarbonyl)-2H-3,7-methanoazacycloundecino(5,4-b)indol-9-yl)-3a,4,5,5a,6,11,12,13a-octahydro-5-hydroxy-8-methoxy-6-methyl-, methyl ester, (3aR-(3aα, 4β, 5β, 5aβ, 9(3R*, 5S*, 7R*, 9S*), 10bR*, 13aα))-; Rozevin; (+)-Vinblastine; Vincaleukoblastine. Grades: >98%. CAS No. 865-21-4. Molecular formula: C46H58N4O9. Mole weight: 810.97. | |
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