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3,5-DIMETHOXY-4-HYDROXYPHENYLMETHYL CARBINOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 33900-62-8 Structure
  • Basic information

    1. Product Name: 3,5-DIMETHOXY-4-HYDROXYPHENYLMETHYL CARBINOL
    2. Synonyms: 3,5-DIMETHOXY-4-HYDROXYPHENYLMETHYL CARBINOL
    3. CAS NO:33900-62-8
    4. Molecular Formula: C10H14O4
    5. Molecular Weight: 198.22
    6. EINECS: N/A
    7. Product Categories: Benzhydrols, Benzyl & Special Alcohols
    8. Mol File: 33900-62-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,5-DIMETHOXY-4-HYDROXYPHENYLMETHYL CARBINOL(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-DIMETHOXY-4-HYDROXYPHENYLMETHYL CARBINOL(33900-62-8)
    11. EPA Substance Registry System: 3,5-DIMETHOXY-4-HYDROXYPHENYLMETHYL CARBINOL(33900-62-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 33900-62-8(Hazardous Substances Data)

33900-62-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33900-62-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,0 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33900-62:
(7*3)+(6*3)+(5*9)+(4*0)+(3*0)+(2*6)+(1*2)=98
98 % 10 = 8
So 33900-62-8 is a valid CAS Registry Number.

33900-62-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-hydroxyethyl)-2,6-dimethoxyphenol

1.2 Other means of identification

Product number -
Other names 3,5-Dimethoxy-4-hydroxyphenylmethyl carbinol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:33900-62-8 SDS

33900-62-8Relevant articles and documents

Efficient cobalt-catalyzed oxidative conversion of lignin models to benzoquinones

Biannic, Berenger,Bozell, Joseph J.

, p. 2730 - 2733 (2013/07/26)

Phenolic lignin model monomers and dimers representing the primary substructural units of lignin were successfully oxidized to benzoquinones in high yield with molecular oxygen using new Co-Schiff base catalysts bearing a bulky heterocyclic nitrogen base as a substituent. This is the first example of a catalytic system able to convert both S and G lignin model phenols in high yield, a process necessary for effective use of lignin as a chemical feedstock.

Fourier transform Raman assignment of guaiacyl and syringyl marker bands for lignin determination

Takayama, Miyuki,Johjima, Toru,Yamanaka, Takeshi,Wariishi, Hiroyuki,Tanaka, Hiroo

, p. 1621 - 1628 (2007/10/03)

A near infrared fourier transform Raman (NIR-FTR) spectroscopic technique was utilized to characterize lignin in wood. The Raman bands for C=C stretching derived from 4-hydroxy-3-methoxyphenyl (guaiacyl) nuclei and from 3,5-dimethoxy-4-hydroxyphenyl (syringyl) nuclei exist independently. The NIR-FTR analysis of a series of lignin model compounds indicated that a syringyl band was shifted to a lower frequency compared to a guaiacyl band. This shift was also observed in chemically synthesized lignin (DHP). Syringyl DHP, in which all the aromatic nuclei consist of syringyl type, exhibited a C=C stretching band at 1594 cm-1, while guaiacyl DHP exhibited the band at 1599 cm-1. These bands were designated as syringyl and guaiacyl marker bands, respectively. Chemical and physical treatment of hardwood and softwood exhibited different characteristics. One of the reasons is the chemical structure of lignin. Softwood mainly contains only guaiacyl lignin, while hardwood contains both guaiacyl and syringyl lignin, and the syringyl/guaiacyl (S/G) ratio varies among species. Under high-resolution conditions (1 cm-1), the NIR-FTR spectra of 10 hardwoods (wood meal samples) revealed that both syringyl and guaiacyl marker bands existed. On the other hand, the spectra of softwoods contained only a guaiacyl marker bands existed. On the other hand, the spectra of softwoods contained only a guaiacyl marker band. The S/G ratio in hardwood calculated from the peak area intensity ratio of two marker bands shows a linear relationship with the S/G ratio obtained from conventional nitrobenzene oxidation analysis with the correlation factor > 0.96. Furthermore, if peak component separation analysis was combined, low-resolution spectral data gave a similar S/G ratio. Either syringyl of guaiacyl marker bands can be assigned in the NIR-FTR spectra of wood blocks (saw-cut surface). This spectral technique may provide an easy-handling and non-destructive analytical method for lignin determination.

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