3,4-Dimethoxybenzyl alcohol, 97%
3,4-Dimethoxybenzyl alcohol, 97%
3,4-Dimethoxybenzyl alcohol, 97%
3,4-Dimethoxybenzyl alcohol, 97%
Thermo Scientific Chemicals

3,4-Dimethoxybenzyl alcohol, 97%

CAS: 93-03-8 | C9H12O3 | 168.192 g/mol
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Catalog number A13396.36
also known as A13396-36
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Quantity:
500 g
Request bulk or custom format
Price (USD)
428.65
Online Exclusive
476.00
Save 47.35 (10%)
Each
Add to cart
Chemical Identifiers
CAS93-03-8
IUPAC Name(3,4-dimethoxyphenyl)methanol
Molecular FormulaC9H12O3
InChI KeyOEGPRYNGFWGMMV-UHFFFAOYSA-N
SMILESCOC1=CC=C(CO)C=C1OC
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SpecificationsSpecification SheetSpecification Sheet
FormLiquid
Refractive Index1.5505-1.5555 @ 20?C
Assay (GC)≥96.0%
Appearance (Color)Clear colorless to yellow to orange
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Suitable for battery materials development.

Applications
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.

Solubility
Fully miscible with water.

Notes
Store in cool, dry place in tightly closed container. Store away from oxidizing agent.
RUO – Research Use Only

General References:

  1. Takahisa Tsukihara; Yoichi Honda; Ryota Sakai; Takahito Watanabe; Takashi Watanabe. Mechanism for oxidation of high-molecular-weight substrates by a fungal versatile peroxidase, MnP2. Applied and Environmental Microbiology. 2008, 74 (9), 2873-2881.
  2. Terhi K Hakala; Kristiina Hildén; Pekka Maijala; Cia Olsson; Annele Hatakka. Differential regulation of manganese peroxidases and characterization of two variable MnP encoding genes in the white-rot fungus Physisporinus rivulosus. Applied Microbiology and Biotechnology, 2006, 73 (4), 839-849.
  3. Reagent for protecting the guanosine residue in oligonucleotide synthesis: Chem. Pharm. Bull., 32, 2882 (1984).