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| Product | Description | |
|---|---|---|
| Vanillin acetate | Vanillin acetate is easily synthesized from vanillin by treatment with acetic anhydride [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 881-68-5. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-W009948. |  |
| Ethylvanillin acetate | Ethyl vanillin acetate is acectate form of ethyl vanillin. Ethyl vanillin acetate is a flavorant used in chocolate or candy [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 72207-94-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-107820. | |
| Acetylvanillin | Acetylvanillin is a derivative of Vanillin, the primary component found in vanilla bean extract. Group: Biochemicals. Alternative Names: NSC 25863; NSC 8499; O-Acetylvanillin; 4-(Acetyloxy)-3-methoxybenzaldehyde; 4-Acetoxy-3-methoxybenzaldehyde; 4-Acetoxy-5-methoxybenzaldehyde; 4-Formyl-2-methoxyphenol Acetate; 4-Formyl-2-methoxyphenyl Acetate; 4-O-Acetylvanillin; 4-(Acetyloxy)-3-methoxybenzaldehyde. Grades: Highly Purified. CAS No. 881-68-5. Pack Sizes: 1g, 5g, 25g, 50g. US Biological Life Sciences. |  Worldwide |
| Vanillin 2',3',4',6'-O-Tetraacetyl-β-D-Glucoside | Vanillin 2',3',4',6'-O-Tetraacetyl-β-D-Glucoside is a protected intermediate in the synthesis of glucosylated precursor of Vanillin found in the seed pods of Vanilla planifola. Synonyms: [(2R,3R,4S,5R,6S)-3,4,5-TRIS(ACETYLOXY)-6-(4-FORMYL-2-METHOXYPHENOXY)OXAN-2-YL]METHYL ACETATE. CAS No. 23598-07-4. Molecular formula: C22H26O12. Mole weight: 482.43. |  |
| (2-Chloro-6-ethoxy-4-formylphenoxy)acetic Acid | (2-Chloro-6-ethoxy-4-formylphenoxy)acetic Acid can be obtained from Ethyl Vanillin (E932100) which is used as a flavorant, which is about three times as potent as vanillin (V097500) and can be utilized in the production of chocolate. Ethyl Vanillin (E932100) has also shown to have antioxidant properties. Group: Biochemicals. Grades: Highly Purified. CAS No. 428836-03-7. Pack Sizes: 100mg, 500mg. Molecular Formula: C11H11ClO5, Molecular Weight: 258.66. US Biological Life Sciences. | Worldwide |
| (2-Ethoxy-4-formylphenoxy)acetic Acid | (2-Ethoxy-4-formylphenoxy)acetic Acid is synthetic reagent, vanillin derivative. It can be used as reagent/reactant for synthetic preparation. Design, synthesis, and biological evaluation of thiazolidine-2,4-dione conjugates as PPAR-γ agonists for use in diabetes treatment. Group: Biochemicals. Grades: Highly Purified. CAS No. 51264-76-7. Pack Sizes: 100mg, 500mg. Molecular Formula: C11H12O5, Molecular Weight: 224.21. US Biological Life Sciences. | Worldwide |
| 3,4-Dimethoxybenzaldehyde | 3,4-Dimethoxybenzaldehyde. Synonyms: Methylvanillin, NSC 24521, NSC 8500, Vanillin methyl ether, Veratraldehyde. CAS No. 120-14-9. Pack Sizes: 5, 100, 500 g in poly bottle. Product ID: CDC10-0173. Molecular formula: (CH3O)2C6H3CHO. Category: Flavoring Chemical Agents. Product Keywords: Cosmetic Ingredients; Flavoring Chemical Agents; 3,4-Dimethoxybenzaldehyde; CDC10-0173; 120-14-9; (CH3O)2C6H3CHO; Methylvanillin, NSC 24521, NSC 8500, Vanillin methyl ether, Veratraldehyde; 204-373-2; MFCD00003363; 120-14-9. Purity: 0.99. Color: White to yellow. EC Number: 204-373-2. Physical State: Solid. Solubility: alcohol: freely soluble. Quality Level: 100. Storage: 2-8°C. Application: 3,4-Dimethoxybenzaldehyde was used in the preparation of 4-chloromethyl-2-(dimethoxyphenyl)-1,3-dioxolane. It was used in the synthesis of (+)-lithospermic acid, having anti-HIV activity. Boiling Point: 281 °C (lit.). Melting Point: 40-43 °C (lit.). Density: 1.1708 (rough estimate). Product Description: 3,4-Dimethoxybenzaldehyde forms 1:1 inclusion complexes with cyclodextrins. It reacts with 3-acetyl-2,5-dimethythiophene to yield chalcone dye, (2E)-3-(3,4-Dimethoxyphenyl)-1-(2,5-dimethylthiophen-3-yl)prop-2-en-1-one. |  |
| 4-O-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)vanillin | 4-O-(2',3',4',6'-tetra-O-acetyl-β-D-glucopyranosyl)vanillin is a compound with remarkable structural and biological properties, used for the research in mitigating an array of afflictions such as cancer, inflammation and microbial infections. Synonyms: Benzaldehyde, 3-methoxy-4-[(2,3,4,6-tetra-o-acetylhexopyranosyl)oxy]-; NSC16965; AC1L5ESY; AC1Q6QED; MolPort-000-452-046; NSC-16965. Grades: 98%. CAS No. 51482-43-0. Molecular formula: C22H26O12. Mole weight: 482.438. | |
| ETHYL VANILLIN HEXYLENE GLYCOL ACETAL | Synonyms: ETHYL VANILLIN HEXYLENE GLYCOL ACETAL, Ethyl vanillin HGA, Phenol, 2-ethoxy-4-(4,4,6-trimethyl-1,3-dioxan-2-yl)- 70-75% [52514-67-7]; 22-27% [107-41-5]; 2-5% [121-32-4], PRODUCT COMPOSITION: 70-75% Ethyl Vanillin Hexylene Glycol Acetal; 22-27% Hexylene Gl. Grades: 70.0% (sum of isomers). CAS No. 52514-67-7. Molecular formula: C15H22O4. Mole weight: 266.11. | |
| Ethyl Vanillin P.G. Acetal | Ethyl Vanillin P.G. Acetal. CAS No. 68527-76-4. FEMA No. 3838. Kosher: Y. VIGON Item # 500722. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Ethyl Vanillin propylene glycol acetal | Ethyl Vanillin propylene glycol acetal. Group: Biochemicals. Grades: Highly Purified. CAS No. 68527-76-4. Pack Sizes: 5g, 10g, 25g, 50g, 100g. US Biological Life Sciences. | Worldwide |
| Vanillin Butylene Glycol Acetal | Vanillin Butylene Glycol Acetal. CAS No. 63253-24-7. FEMA No. 4023. Kosher: Y. VIGON Item # 501999. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| vanillin synthase | Involved, together with EC 4.2.1.101 trans-feruloyl-CoA hydratase, in the production of vanillin from trans-ferulic acid. Vanillin is converted to vanillate by EC 1.2.1.67 vanillin dehydrogenase. Group: Enzymes. Synonyms: 3-hydroxy-3-(4-hydroxy-3-methoxyphenyl)propionyl-CoA:vanillin lyase (acetyl-CoA-forming). Enzyme Commission Number: EC 4.1.2.41. CAS No. 449168-60-9. 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-4877; vanillin synthase; EC 4.1.2.41; 449168-60-9; 3-hydroxy-3-(4-hydroxy-3-methoxyphenyl)propionyl-CoA:vanillin lyase (acetyl-CoA-forming). Cat No: EXWM-4877. |  |
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