| Identification | More | [Name]
1,3-Dimethoxybenzene | [CAS]
151-10-0 | [Synonyms]
1,3-DIMETHOXYBENZENE
3-METHOXYANISOLE
DIMETHYLRESORCINOL
FEMA 2385
M-DIMETHOXYBENZENE
M-METHOXYANISOLE
M-PHENYLENEDIMETHYL ETHER
RESCORCINOL DIMETHYL ETHER
RESORCINOL DIMETHYL ETHER
1,3-dimethoxy-benzen
Benzene, m-dimethoxy-
Benzene,1,3-dimethoxy-
Dimethylether resorcinolu
dimethyletherresorcinolu
Dimethylresorinol
m-dimethoxy-benzen
1,3-Dimethoxybenzeen
Dimethylether resorcinolu (Czech)
1，3-dimethyoxy benzene
Resorcinol dimethlyether | [EINECS(EC#)]
205-783-4 | [Molecular Formula]
C8H10O2 | [MDL Number]
MFCD00008384 | [Molecular Weight]
138.16 | [MOL File]
151-10-0.mol |
| Chemical Properties | Back Directory | [Appearance]
clear colorless to slightly brown liquid | [Melting point ]
-52°C | [Boiling point ]
85-87 °C7 mm Hg(lit.)
| [density ]
1.055 g/mL at 25 °C(lit.)
| [FEMA ]
2385 | [refractive index ]
n20/D 1.524(lit.)
| [Fp ]
190 °F
| [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Miscible with toluene. | [form ]
Liquid | [color ]
Clear colorless to slightly brown | [Odor]
at 1.00 % in dipropylene glycol. acid fruity nutmeg neroli | [biological source]
synthetic | [Odor Type]
medicinal | [Water Solubility ]
1.216g/L(25 ºC) | [JECFA Number]
1249 | [BRN ]
878582 | [Dielectric constant]
4.5（23.0℃） | [Cosmetics Ingredients Functions]
PERFUMING | [InChI]
1S/C8H10O2/c1-9-7-4-3-5-8(6-7)10-2/h3-6H,1-2H3 | [InChIKey]
DPZNOMCNRMUKPS-UHFFFAOYSA-N | [SMILES]
COc1cccc(OC)c1 | [LogP]
2.21 | [Uses]
Organic intermediate, flavoring.
| [CAS DataBase Reference]
151-10-0(CAS DataBase Reference) | [NIST Chemistry Reference]
Benzene, 1,3-dimethoxy-(151-10-0) | [EPA Substance Registry System]
151-10-0(EPA Substance) |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H227 | [Precautionary statements ]
P261-P280h-P210-P280-P370+P378-P403+P235-P501 | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [RIDADR ]
NA 1993 / PGIII | [WGK Germany ]
2
| [RTECS ]
CZ6474000
| [Hazard Note ]
Irritant | [TSCA ]
Yes | [REACH Registrations]
Active | [HS Code ]
29093090 | [Storage Class]
10 - Combustible liquids | [Toxicity]
mouse,LD50,intraperitoneal,900mg/kg (900mg/kg),BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)BEHAVIORAL: ATAXIABEHAVIORAL: TREMOR,Journal of the American Pharmaceutical Association, Scientific Edition. Vol. 46, Pg. 185, 1957. |
| Hazard Information | Back Directory | [Description]
1,3-Dimethoxybenzene, also known as dimethyl resorcinol or 3-methoxyanisole, belongs to the class of organic compounds known as dimethoxybenzenes. These organic aromatic compounds contain a monocyclic benzene moiety carrying two methoxy groups. 1,3-Dimethoxybenzene has been used in the synthesis of novel oxathiane spiroketal donors. It forms pi- and O-ylidic complexes with dichlorocarbene (CCl(2)).
| [Chemical Properties]
clear colorless to slightly brown liquid | [Chemical Properties]
m-Dimethoxybenzene has a very powerful sweet-earthy, intensely, nut-like aroma. | [Occurrence]
Reported found in Gruyere de Comte, blue cheeses, filberts and cognac | [Definition]
ChEBI: 1,3-Dimethoxybenzene is a member of methoxybenzenes. | [Preparation]
From resorcinol by methylation using dimethyl sulfate and alka | [Production Methods]
1,3-Dimethoxybenzene can be produced 1) by Methylation of Resorcinol in weak
aqueous alkali with Dimethylsulfate.
2) from Methanol and Resorcinol with Potassium hydrosuIfate or Sodium naphthalene sulfonate as dehydrating agent. | [Taste threshold values]
Chemical, medicinal, spice, cooling root beer-like. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 55, p. 991, 1990 DOI: 10.1021/jo00290a033 | [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. | [Purification Methods]
Extract it with aqueous NaOH, and water, then dry it. Fractionally distil it from BaO or Na. [Beilstein 6 IV 5663.] |
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