ChemicalBook > CAS DataBase List > 3,5-Dimethoxytoluene

3,5-Dimethoxytoluene

Product Name
3,5-Dimethoxytoluene
CAS No.
4179-19-5
Chemical Name
3,5-Dimethoxytoluene
Synonyms
1,3-Dimethoxy-5-methylbenzene;SKL305;3,5-DIMETHOXYTOLUENE;ORCINOL DIMETHYL ETHER;Toluene, 3,5-dimethoxy-;3,5-Dimethoxytoluene,99%;3,5-Dimethoxytoluene >3,5-DiMethoxytoluene, GC 98%;1,3-dimethoxy-5-methyl-benzen;3,5-Dimethoxy-1-methylbenzene
CBNumber
CB0230254
Molecular Formula
C9H12O2
Formula Weight
152.19
MOL File
4179-19-5.mol
More
Less

3,5-Dimethoxytoluene Property

Melting point:
61-62 C
Boiling point:
244 °C (lit.)
Density 
1.039 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.522(lit.)
Flash point:
215 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Sparingly), Methanol (Sparingly)
form 
Liquid
Specific Gravity
1.039
color 
Clear colorless to yellow
Odor
Warm and sweet, nut-like, earthy-mossy odor
BRN 
2043558
LogP
2.897 (est)
CAS DataBase Reference
4179-19-5(CAS DataBase Reference)
NIST Chemistry Reference
3,5-Dimethoxytoluene(4179-19-5)
EPA Substance Registry System
3,5-Dimethoxytoluene (4179-19-5)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
TSCA 
Yes
HS Code 
29093090
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
423742
Product name
3,5-Dimethoxytoluene
Purity
98%
Packaging
1g
Price
$20.52
Updated
2024/03/01
TCI Chemical
Product number
D2526
Product name
3,5-Dimethoxytoluene
Purity
>97.0%(GC)
Packaging
5g
Price
$47
Updated
2024/03/01
TCI Chemical
Product number
D2526
Product name
3,5-Dimethoxytoluene
Purity
>97.0%(GC)
Packaging
25g
Price
$186
Updated
2024/03/01
Alfa Aesar
Product number
L00809
Product name
3,5-Dimethoxytoluene, 98%
Packaging
1g
Price
$35.65
Updated
2024/03/01
Alfa Aesar
Product number
L00809
Product name
3,5-Dimethoxytoluene, 98%
Packaging
5g
Price
$102.65
Updated
2024/03/01
More
Less

3,5-Dimethoxytoluene Chemical Properties,Usage,Production

Chemical Properties

Clear colorless to yellow liquid

Uses

3,5-Dimethoxytoluene (DMT) may be used in the synthesis of 3,5-dimethoxybenzoic acid by oxidation and 2-methoxy-6-methyl-1,4-benzoquinone by catalytic oxidation with hydrogen peroxide (H2O2)/methyltrioxorhenium (CH3ReO3) in dimethyl carbonate (DMC).

Uses

3,5-Dimethoxytoluene has been suggested for use in perfume compositions as supporting note for Oakmoss and Vetiver, and as a novel note in Chypre, Fougere and Oriental fragrance types.

Definition

ChEBI: 3,5-dimethoxytoluene is a member of the class of toluenes that is toluene in which the hydrogens at positions 3 and 5 have been replaced by methoxy groups. It is the major scent compound of many rose varieties. It has a role as a fragrance and a plant metabolite. It is a member of toluenes and a member of methoxybenzenes.

Production Methods

3,5-Dimethoxytoluene can be produced from Orcinol in weak aqueous alkali with Dimethylsulfate at controlled temperature.

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 6, p. 859, 1988
The Journal of Organic Chemistry, 70, p. 3275, 2005 DOI: 10.1021/jo050075r

General Description

3,5-Dimethoxytoluene (DMT) is a methoxylated phenolic derivative. It is reported to be one of the main constituent of the floral volatiles in different rose varieties. It has been biosynthesized from orcinol by two successive methylation catalyzed by O-methyltransferases (OMTs). The features of its aerobic oxidation with metal/bromide catalysts have been investigated.

Synthesis

A solution of dry orcinol (14.2 g,0.115 mole) in dry anhydrous acetone(150 ml) containing anhydrous potassium carbonate (45 g) is refluxed withdimethyl sulphate (23.6 ml,31.46 g, 0.25 mole) for 4 hr. The dimethylsulphate is added in small lots of 5 ml. After refluxing, the solution isfiltered and the inorganic residue washed with hot acetone (2 x 25 ml).The combined acetone solution is distilled and the residue macerated withcrushed ice. It is extracted with ether, the ether extract dried (anhydroussodium sulphate) and distilled. Yield 14.2 g (81.6%).B.p.102° (8 mm)

3,5-Dimethoxytoluene Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

3,5-Dimethoxytoluene Suppliers

TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32165
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
TargetMol Chemicals Inc.
Tel
Email
support@targetmol.com
Country
United States
ProdList
38632
Advantage
58
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
Leonid Chemicals Private Limited
Tel
--
Fax
--
Email
careers@leonidchemicals.com
Country
United States
ProdList
1700
Advantage
43
Penta International Corporation
Tel
--
Fax
--
Email
lisaa@pentamfg.com
Country
United States
ProdList
5042
Advantage
58
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Youth (Shanghai) Chemical Technology Co., Ltd.
Tel
--
Fax
--
Email
sales_youthchem@163.com
Country
United States
ProdList
55
Advantage
0
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6962
Advantage
56
Penta Manufacturing Company
Tel
--
Fax
--
Email
sales@pentamfg.com
Country
United States
ProdList
5076
Advantage
65
Beta Pharma, Inc.
Tel
--
Fax
--
Email
sales@betapharma.com
Country
United States
ProdList
6226
Advantage
60
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
United States
ProdList
6814
Advantage
81
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
More
Less

View Lastest Price from 3,5-Dimethoxytoluene manufacturers

Zhuozhou Wenxi import and Export Co., Ltd
Product
3,5-Dimethoxytoluene 4179-19-5
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-08-11
Zhuozhou Wenxi import and Export Co., Ltd
Product
3,5-Dimethoxytoluene 4179-19-5
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-06-27
Career Henan Chemical Co
Product
3,5-DIMETHOXYTOLUENE 4179-19-5
Price
US $1.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
200KG
Release date
2020-01-09

4179-19-5, 3,5-DimethoxytolueneRelated Search:


  • 3,5-DIMETHOXYTOLUENE
  • 3,5-DiMethoxytoluene, GC 98%
  • ORCINOL DIMETHYL ETHER
  • 3,5-Dimethoxy-1-methylbenzene
  • 5-Methylresorcinol dimethyl ether
  • Benzene, 1,3-dimethoxy-5-methyl-
  • Toluene, 3,5-dimethoxy-
  • 1,5-Dimethoxy-3-methylbenzene
  • 5-Methyl-1,3-dimethoxybenzene
  • 3,5-Dimethoxytoluene,99%
  • 1,3-dimethoxy-5-methyl-benzen
  • 1,3-Dimethoxy-5-methylbenzene
  • 1,3-dimethoxy-5-methyl-Benzene
  • 3,5-Dimethoxytoluene &gt
  • SKL305
  • 3,5-Dimethoxytoluene, ≥ 97.0%
  • Orcinol dimethyl ether|||1,3-dimethoxy-5-methylbenzene
  • 4179-19-5
  • CH3C6H3OCH32
  • Ethers
  • Oxygen Compounds
  • Organic Building Blocks
  • Building Blocks
  • Building Blocks
  • C9
  • Aromatic Ethers
  • Ethers
  • Organic Building Blocks
  • Oxygen Compounds
  • Chemical Synthesis
  • Organic Building Blocks
  • Oxygen Compounds