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Home > products > Chemical Intermediates > 2,6-Dimethylphenol CAS 576-26-1

2,6-Dimethylphenol CAS 576-26-1

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 576-26-1

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Highlight:
CAS NO::
576-26-1
Appearance::
White Crystal
Molecular Formula: Appearance::
C8H10O
Molecular Weight::
122.1640
EINECS NO::
209-400-1
MDL NO::
MFCD00002240
CAS NO::
576-26-1
Appearance::
White Crystal
Molecular Formula: Appearance::
C8H10O
Molecular Weight::
122.1640
EINECS NO::
209-400-1
MDL NO::
MFCD00002240
2,6-Dimethylphenol CAS 576-26-1

Product Description:

Product Name: 2,6-Dimethylphenol CAS NO: 576-26-1

 

 

 

 

 

 

 

Synonyms:

2,6-Me2C6H3OH;

2-hydroxy-1,3-dimethylbenzene;

2,6-dimethylphenethyl chloride;

 

 

 

 

 

 

 

 

 

Chemical & Physical Properties:

Appearance: White crystal

Assay :≥99.0%

Density: 1.15

Boiling Point: 203℃

Melting Point: 44-46℃

Flash Point: 73℃

Refractive Index: 1.5148 (65℃)

Water Solubility: 10 g/L (20 ℃)

Stability: Stable. Very flammable. Incompatible with oxidizing agents, acid chlorides, acid anhydrides, steel, copper, copper alloys, bases, acid chlorides.

Storage Condition: Keep away from heat, sparks, and flame. Keep away from sources of ignition. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

 

 

 

 

 

 

 

 

 

Safety Information:

RTECS: ZE6125000

Hazard Class: 6.1

Safety Statements: S26-S36/37/39-S45-S61

HS Code: 29071400

Packing Group: II

WGK Germany: 2

RIDADR: UN 2261

Risk Statements: R24/25; R34; R51/53

Hazard Codes: T; N

 

 

 

 

 

 

 

 

2,6-Xylenol is a chemical compound which is one of the six isomers of xylenol. It is also commonly known as 2,6-dimethylphenol (DMP).

 

 

2,6-Xylenol is a monomer for poly(p-phenylene oxide) engineering resins through carbon - oxygen oxidative coupling. Carbon to carbon dimerization is also possible. In one study 2,6-xylenol is oxidized with iodosobenzene diacetate with an 5 fold excess of the phenol.

 

 

In the first step of the proposed reaction mechanism the acetyl groups in the iodine compound are replaced with the phenol. This complex dissociates into an aryl radical anion and a phenoxy residue. The two aryl radicals recombine forming a new carbon carbon covalent bond and subsequently lose two protons in a rearomatization step. The immediate reaction product is a diphenoquinone as result of a one-step 4-electron oxidation. It is nevertheless possible to synthesize the biphenol compound via a comproportionation of the quinone with xylenol already present. In this reaction sequence the hypervalent iodine reagent is eventually reduced to phenyliodine. 2-hydroxy-1,3-dimethylbenzene is used in the production of polyphenyl eth er resins, photographic agents, pesticides, polyester and polyether resins. 2,6-Me-PhOH can make the antiarrhythmic drug bradycardia. 2,6-dimethylphenethyl chloride is used in organic synthesis and antisepsis, medicine, solvents and antioxidants.

 

 

 

 

 

 

 

 

 

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