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2,5-DIMETHYLANISOLE

CAS No.
1706-11-2
Chemical Name:
2,5-DIMETHYLANISOLE
Synonyms
2-METHOXY-P-XYLENE;3-Methoxy-p-xylene;2,5-DIMETHYLANISOLE;3,6-Dimethylanisole;2,5-Dimethylanisole>2,5-Dimethylanisole,99%;2,5-Dimethylanisole 99%;2,5-DIMETHYLANISOLE, 98+%;1,4-DIMETHYL-2-METHOXYBENZENE;2-Methoxy-1,4-dimethylbenzene
CBNumber:
CB5126350
Molecular Formula:
C9H12O
Molecular Weight:
136.19
MDL Number:
MFCD00008378
MOL File:
1706-11-2.mol
MSDS File:
SDS
Last updated:2026-05-28 01:24:15
Product description Number Pack Size Price
2,5-Dimethylanisole 99% 137480 25g $150
2,5-Dimethylanisole >98.0%(GC) D2440 25g $73
2,5-Dimethylanisole, min. 98% min.98% 06-0069 25g $120
2,5-Dimethylanisole, min. 98% min.98% 06-0069 100g $360
2,5-Dimethylanisole BAA70611 0.25g $250
More product size

2,5-DIMETHYLANISOLE Properties

Melting point 90-92 °C
Boiling point 190 °C (lit.)
Density 0.965 g/mL at 25 °C (lit.)
refractive index n20/D 1.514(lit.)
Flash point 151 °F
storage temp. Sealed in dry,Room Temperature
form clear liquid
color Colorless to Almost colorless
Specific Gravity 0.965
BRN 774604
InChI 1S/C9H12O/c1-7-4-5-8(2)9(6-7)10-3/h4-6H,1-3H3
InChIKey SJZAUIVYZWPNAS-UHFFFAOYSA-N
SMILES COc1cc(C)ccc1C
CAS DataBase Reference 1706-11-2(CAS DataBase Reference)
FDA UNII RH47BOM48G
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
Signal word  Danger
Hazard statements  H227-H302-H315-H318-H335
Precautionary statements  P261-P280-P305+P351+P338-P210e-P280a-P370+P378a-P501a-P210-P370+P378-P403+P235-P501
Hazard Codes  Xn
Risk Statements  22-37/38-41
Safety Statements  24/25-26
WGK Germany  3
HS Code  29093090
Storage Class 10 - Combustible liquids
NFPA 704
1
0 0

2,5-DIMETHYLANISOLE price More Price(35)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 137480 2,5-Dimethylanisole 99% 1706-11-2 25g $150 2026-04-30 Buy
TCI Chemical D2440 2,5-Dimethylanisole >98.0%(GC) 1706-11-2 25g $73 2026-04-30 Buy
Strem Chemicals 06-0069 2,5-Dimethylanisole, min. 98% min.98% 1706-11-2 25g $120 2026-04-30 Buy
Strem Chemicals 06-0069 2,5-Dimethylanisole, min. 98% min.98% 1706-11-2 100g $360 2026-04-30 Buy
Biosynth BAA70611 2,5-Dimethylanisole 1706-11-2 0.25g $250 2026-06-04 Buy
Product number Packaging Price Buy
137480 25g $150 Buy
D2440 25g $73 Buy
06-0069 25g $120 Buy
06-0069 100g $360 Buy
BAA70611 0.25g $250 Buy

2,5-DIMETHYLANISOLE Chemical Properties,Uses,Production

Chemical Properties

CLEAR COLOURLESS TO SLIGHTLY YELLOWISH LIQUID

Uses

2,5-Dimethylanisole was used to investigate the temperature dependence of spin-rotational relaxation rate of methyl C-13 in 2, 5-dimethylaniline.

General Description

2,5-Dimethylanisole acts as photoexcited donor and undergoes different non-radiative transitions in the presence of the acceptor 2-nitrofluorene in ethanol rigid glassy matrix at 77K.

Synthesis

2,5-Dimethylphenol

95-87-4

Dimethyl sulfate

77-78-1

2,5-DIMETHYLANISOLE

1706-11-2

General procedure for the synthesis of 2,5-dimethylanisole from 2,5-dimethylphenol and dimethyl sulfate: Step 1: 2,5-dimethylphenol (50 g, 410 mmol) and potassium carbonate (68 g, 490 mmol) were dissolved in acetone (600 mL) at room temperature, followed by the addition of dimethyl sulfate (31.02 g, 246 mmol). The reaction mixture was heated and refluxed for 9 h. The progress of the reaction was monitored by TLC and it was found that the starting material was still present. Dimethyl sulfate (31.02 g, 246 mmol) was added additionally and the reaction was continued to reflux for 9 hours. Upon completion of the reaction, the mixture was filtered and acetone was removed using a rotary evaporator. The resulting oil was stirred with 20% sodium hydroxide solution (100 mL) for 10 minutes. The organic layer was washed with water (2 x 500 mL) until the aqueous layer was neutral. The organic layer was dried over sodium sulfate and concentrated in vacuum to give 45.5 g of 2-methoxy-1,4-dimethylbenzene in 81% yield. 1H NMR (CDCl3) δ ppm: 2.2 (3H, s, CH3), 2.34 (3H, s, CH3), 3.82 (3H, s, OCH3), 6.65 (1H, s, Ar-H), 6.7 (1H, d, J = 7.2Hz, Ar-H), 7.03 (1H, d, J = 7.2Hz, Ar-H).

References

[1] Patent: WO2010/59549, 2010, A1. Location in patent: Page/Page column 18-19
[2] Phosphorus, Sulfur and Silicon and the Related Elements, 2005, vol. 180, # 7, p. 1701 - 1712
[3] Journal fuer Praktische Chemie (Leipzig), 1928, vol. <2> 119, p. 351
[4] Journal of the Chemical Society, 1929, p. 2368
[5] Journal of the Chemical Society, 1930, p. 1110

95-87-4
77-78-1
1706-11-2
Synthesis of 2,5-DIMETHYLANISOLE from 2,5-Dimethylphenol and Dimethyl sulfate
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View Lastest Price from 2,5-DIMETHYLANISOLE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,5-DIMETHYLANISOLE pictures 2026-03-20 2,5-DIMETHYLANISOLE
1706-11-2
1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
2,5-DIMETHYLANISOLE pictures 2024-04-24 2,5-DIMETHYLANISOLE
1706-11-2
$50.00 1kg 99.10% 50000kg Ouhuang Engineering Materials (Hubei) Co., Ltd
2,5-DiMethylanisole pictures 2022-01-15 2,5-DiMethylanisole
1706-11-2
1KG 98.7% 100 tons Honest Joy Holdings Limited
3-Methoxy-p-xylene 2,5-Dimethylanisole,99% 2,5-DIMETHYLANISOLE FOR SYNTHESIS 2,5-Dimethylanisole 99% 2-Methoxy-1,4-dimethylbenzene Benzene, 1-methoxy-2,5-dimethyl Benzene, 2-methoxy-1,4-dimethyl- 2-METHOXY-P-XYLENE 2,5-DIMETHYLANISOLE 1,4-DIMETHYL-2-METHOXYBENZENE 2,5-DIMETHYLANISOLE, 98+% 5-(2,3,4-trimethoxyphenyl)-1,3,4-oxadiazol-2-amine 2,5-Dimethylanisole> 3,6-Dimethylanisole 1706-11-2 Building Blocks Oxygen Compounds Organic Building Blocks Ethers Building Blocks C9 Chemical Synthesis Organic Building Blocks Oxygen Compounds Ethers Organic Building Blocks Oxygen Compounds Aromatic Ethers Anisoles, Alkyloxy Compounds & Phenylacetates