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Key Documents

132632

Sigma-Aldrich

3,5-Dimethoxyphenol

99%

Synonym(s):

Phloroglucinol dimethyl ether

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About This Item

Linear Formula:
(CH3O)2C6H3OH
CAS Number:
Molecular Weight:
154.16
Beilstein:
1239156
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

solid

bp

172-175 °C/17 mmHg (lit.)

mp

40-43 °C (lit.)

SMILES string

COc1cc(O)cc(OC)c1

InChI

1S/C8H10O3/c1-10-7-3-6(9)4-8(5-7)11-2/h3-5,9H,1-2H3

InChI key

XQDNFAMOIPNVES-UHFFFAOYSA-N

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Application

3,5-Dimethoxyphenol has been used in a study on iron porphyrin phenoxides. It was used to develop a new analytical method using LC-MS that enables the simultaneous identification and quantification of new alkaloids and the alkaloidal diterpenoids.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Iron porphyrin phenoxides: models for some hemoglobin mutants.
Ainscough E_W, et al.
Journal of the American Chemical Society, 100(24), 7585-7591 (1978)
Laura Burga et al.
Archives of biochemistry and biophysics, 440(1), 54-64 (2005-07-19)
A cDNA was cloned from Ruta graveolens cells encoding a novel O-methyltransferase (OMT) with high similarity to orcinol or chavicol/eugenol OMTs, but containing a serine-rich N-terminus and a 13 amino acid insertion between motifs IV and V. Expression in Escherichia
R Froldi et al.
Journal of analytical toxicology, 34(1), 53-56 (2010-01-30)
Taxus baccata is a widely distributed yew often associated with cases of fatal intoxication, which is related to the high amounts of cardiotoxic alkaloids, taxine A and taxine B, contained in its leaves. In this paper, a case of Taxus
Márcia Pessêgo et al.
Journal of pharmacy & bioallied sciences, 3(1), 128-134 (2011-03-25)
Nitrosative deamination of DNA bases induced by reaction with reactive nitrogen species (RNS) has been pointed out as a probable cause of mutagenesis. (Poly)phenols, present in many food items from the Mediterranean diet, are believed to possess antinitrosating properties due
Modern analytical procedures for the determination of taxus alkaloids in biological material.
F Musshoff et al.
International journal of legal medicine, 122(4), 357-358 (2008-05-07)

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