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MilliporeSigma

132632

3,5-Dimethoxyphenol

99%

Synonym(s):

Phloroglucinol dimethyl ether

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About This Item

Linear Formula:
(CH3O)2C6H3OH
CAS Number:
500-99-2
Molecular Weight:
154.16
Beilstein/REAXYS Number:
1239156
EC Number:
207-917-7
MDL number:
MFCD00008388
UNSPSC Code:
12352100
PubChem Substance ID:
24848062
NACRES:
NA.22

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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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1 of 4

This Item
D135550D133809EX0185
3,5-Dimethoxyphenol 99%

Sigma-Aldrich

132632

3,5-Dimethoxyphenol

2,6-Dimethoxyphenol 99%

Sigma-Aldrich

D135550

2,6-Dimethoxyphenol

3,4-Dimethoxycinnamic acid, predominantly trans 99%

Sigma-Aldrich

D133809

3,4-Dimethoxycinnamic acid, predominantly trans

Ethyl Ether Meets ACS Specifications, Meets Reagent Specifications for testing USP/NF monographs GR ACS

Supelco

EX0185

Ethyl Ether

assay

99%

assay

99%

assay

99%

assay

≥98.0% ethanol basis (diethyl ether)

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

200

bp

172-175 °C/17 mmHg (lit.)

bp

261 °C (lit.)

bp

-

bp

34.6 °C (lit.)

form

solid

form

solid

form

powder

form

liquid

mp

40-43 °C (lit.)

mp

50-57 °C (lit.)

mp

181-183 °C (lit.)

mp

−116 °C (lit.)

Application

3,5-Dimethoxyphenol has been used in a study on iron porphyrin phenoxides[1]. 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[2].

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN7187
BCCL3468
BCBB2917
BCBB2918V
BCBB2917V

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Claudia Panzeri et al.
Clinical toxicology (Philadelphia, Pa.), 48(5), 463-465 (2010-06-10)
Yew (Taxus baccata) is a conifer known to be toxic since ancient times. Taxine A and taxine B, the toxic alkaloids of Taxus, block cardiac sodium and calcium channels causing nausea, vomiting, abdominal pain, cardiac arrhythmias, respiratory distress, coma, seizures
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
J Stríbrný et al.
Soudni lekarstvi, 55(3), 36-39 (2010-10-15)
Autopsy findings of fatal intoxication with yew (Taxus baccata) are nonspecific. A presence of plant residues in the digestive tract can signalize yew intoxication. If yew decoction is consumed, plant residues are not found. In such a case the intoxication
Iron porphyrin phenoxides: models for some hemoglobin mutants.
Ainscough E_W, et al.
Journal of the American Chemical Society, 100(24), 7585-7591 (1978)
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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