- Veratryl alcohol
-
- $39.00
-
2026-06-16
- CAS:93-03-8
- Purity: 99.94%
- Supply Ability: 10g
- Veratryl alcohol
-
- $39.00
-
2026-06-16
- CAS:93-03-8
- Purity: 99.94%
- Supply Ability: 10g
- Veratryl alcohol
-
- $39.00
-
2026-06-16
- CAS:93-03-8
- Purity: 99.94%
- Supply Ability: 10g
|
| | 3,4-Dimethoxybenzyl alcohol Basic information |
| Product Name: | 3,4-Dimethoxybenzyl alcohol | | Synonyms: | 3,4-dimethoxy-Benzenemethanol;3,4-Dimethoxyphenylmethyl alcohol;RARECHEM AL BD 0062;3,4-Dimethoxybenzene-1-methanol;3,4-Dimethoxybenzyl alcohol,96%;3,4-DIMETHOXYBENZYL ALCOHOL / VERATRYL ALCOHOL;3,4-DIMETHOXYBENZYL ALCOHOL 98%;3,4-DIMETHOXYBENZYL ALCOHOL | | CAS: | 93-03-8 | | MF: | C9H12O3 | | MW: | 168.19 | | EINECS: | 202-212-0 | | Product Categories: | Aromatics, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals;Alkohols;Benzhydrols, Benzyl & Special Alcohols | | Mol File: | 93-03-8.mol |  |
| | 3,4-Dimethoxybenzyl alcohol Chemical Properties |
| Melting point | 22 °C | | Boiling point | 296-297 °C732 mm Hg(lit.) | | density | 1.157 g/mL at 25 °C(lit.) | | refractive index | n20/D 1.552(lit.) | | Fp | >230 °F | | storage temp. | Inert atmosphere,Room Temperature | | solubility | Chloroform (Slightly), Methanol (Slightly) | | form | Oily Liquid | | pka | 14.18±0.10(Predicted) | | color | Clear colorless to yellow or golden | | Water Solubility | miscible | | BRN | 639388 | | Cosmetics Ingredients Functions | SKIN CONDITIONING | | InChI | 1S/C9H12O3/c1-11-8-4-3-7(6-10)5-9(8)12-2/h3-5,10H,6H2,1-2H3 | | InChIKey | OEGPRYNGFWGMMV-UHFFFAOYSA-N | | SMILES | COc1ccc(CO)cc1OC | | LogP | 0.72 | | CAS DataBase Reference | 93-03-8(CAS DataBase Reference) | | NIST Chemistry Reference | Benzenemethanol, 3,4-dimethoxy-(93-03-8) | | EPA Substance Registry System | Benzenemethanol, 3,4-dimethoxy- (93-03-8) |
| Hazard Codes | Xn,Xi | | Risk Statements | 22-36/37/38 | | Safety Statements | 24/25-36/37-26 | | WGK Germany | 3 | | TSCA | TSCA listed | | HS Code | 29062990 | | Storage Class | 10 - Combustible liquids |
| | 3,4-Dimethoxybenzyl alcohol Usage And Synthesis |
| Chemical Properties | Colorless to light yellow liqui | | Uses | 3,4-Dimethoxybenzyl Alcohol is a secondary metabolite of some lignin degrading fungi. Recent studies have been conducted to explore whether 3,4-Dimethoxybenzyl Alcohol, a product from the biodegradati
on of lignocellulosic biomass, could be used as the fuel of the microbial fuel cell (MFC) to generate power. | | Uses | 3,4-Dimethoxybenzyl alcohol used as the fuel of the microbial fuel cell (MFC) to generate power. Veratrole alcohol is the raw material for the synthesis of cyclotriveratrylene which is used in host-guest chemistry. | | Uses | 3,4-Dimethoxybenzyl alcohol is widely used in the synthesis of various cyclotriveratrylenes (CTVs), which are cyclic molecular hosts with a cavity to accommodate guest molecules. It can also be used as a precursor in the total synthesis of salvianolic acid N. | | Definition | ChEBI:
(3,4-dimethoxyphenyl)methanol is a member of the class of benzyl alcohols that is benzyl alcohol in which the hydrogens at positions 3 and 4 of the phenyl group are substituted by methoxy groups. It has a role as a fungal metabolite. It is a member of benzyl alcohols, a primary alcohol and a dimethoxybenzene. | | Synthesis Reference(s) | Chemical and Pharmaceutical Bulletin, 34, p. 4109, 1986 DOI: 10.1248/cpb.34.4109
The Journal of Organic Chemistry, 59, p. 7138, 1994 DOI: 10.1021/jo00102a048 | | General Description | Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. | | Synthesis | Using 3,4-dimethoxybenzaldehyde as a raw material, reduction is carried out in methanol or other alcohol solvents by adding sodium borohydride (a mild reducing agent commonly used in industry), with the reaction stirred at room temperature to reflux temperature; or in the laboratory, lithium aluminum hydride (in anhydrous tetrahydrofuran or diethyl ether) can be used for reduction. After the reaction is completed, the product 3,4-dimethoxybenzyl alcohol is obtained by acidification, extraction, drying, distillation or recrystallization. |
| | 3,4-Dimethoxybenzyl alcohol Preparation Products And Raw materials |
|