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W238503

Sigma-Aldrich

1,3-Dimethoxybenzene

≥98%, FG

Synonym(s):

Dimethylresorcinol, Resorcinol dimethyl ether

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About This Item

Linear Formula:
C6H4(OCH3)2
CAS Number:
Molecular Weight:
138.16
FEMA Number:
2385
Beilstein:
878582
EC Number:
Council of Europe no.:
189
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
4.016
NACRES:
NA.21

biological source

synthetic

Quality Level

grade

FG
Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines
meets purity specifications of JECFA

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117

Assay

≥98%

refractive index

n20/D 1.524 (lit.)

bp

85-87 °C/7 mmHg (lit.)

density

1.055 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

Organoleptic

medicinal; chemical; cooling; sweet

SMILES string

COc1cccc(OC)c1

InChI

1S/C8H10O2/c1-9-7-4-3-5-8(6-7)10-2/h3-6H,1-2H3

InChI key

DPZNOMCNRMUKPS-UHFFFAOYSA-N

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General description

1,3-Dimethoxybenzene can be used as a flavoring agent in the food industry. It is reported to be found in the volatiles of port wine and Roquefort cheese.

Application


  • Homogeneous Gold Catalysis Using Complexes Recovered from Waste Electronic Equipment.: This research utilizes 1,3-Dimethoxybenzene in catalytic processes involving gold complexes reclaimed from electronic waste, presenting a sustainable approach in catalytic chemistry and highlighting the reuse of precious metals in industrial applications (McCarthy et al., 2022).

  • Sequential Ir/Cu-Mediated Method for the Meta-Selective C-H Radiofluorination of (Hetero)Arenes.: Demonstrates a technique for the meta-selective C-H radiofluorination involving 1,3-Dimethoxybenzene, offering a novel pathway for the synthesis of radio-labelled compounds used in PET imaging, which is crucial for medical diagnostics and research (Wright et al., 2021).

  • Synthesis and antioxidant activities of phenol derivatives from 1,6-bis(dimethoxyphenyl)hexane-1,6-dione.: Discusses the synthesis of new antioxidant compounds derived from 1,3-Dimethoxybenzene, underlining its role in developing therapeutic agents that could mitigate oxidative stress-related diseases (Artunc et al., 2020).

  • One-Step Synthesis of C(2v)-Symmetric Resorcin[4]arene Tetraethers.: This paper details a one-step synthesis method using 1,3-Dimethoxybenzene to create novel macrocyclic molecules, potentially useful in host-guest chemistry and molecular recognition, which are key areas in supramolecular chemistry and nanotechnology (Smith et al., 2020).

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

190.4 °F - closed cup

Flash Point(C)

88 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Burdock, GA
Encyclopedia of Food and Color Additives, 1, 839-840 (1997)
Burdock, GA
Encyclopedia of Food and Color Additives, 1, 839-840 (1997)
Helena Zahradnícková et al.
Journal of separation science, 29(2), 236-241 (2006-03-10)
For the first time, headspace solid-phase microextraction coupled with GC-MS analysis was used to study volatile compounds emitted by the tick Ixodes ricinus (L.). Variables such as the type of SPME fibre, equilibration time and extraction time have been evaluated
1, 3?Dimethoxybenzene, a newly identified component of port wine.
Rogerson FSS, et al.
Journal of the Science of Food and Agriculture, 82(11), 1287-1292 (2002)
Takashi Iijima et al.
Bioscience, biotechnology, and biochemistry, 73(11), 2547-2548 (2009-11-10)
An efficient synthesis of tri-O-methylated resveratrol is presented using an advanced Heck reaction promoted by Pd(dba)(2) in the presence of P(t-Bu)(3).

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