Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 576-26-1
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Aluminum Foil Bag, Drum
Delivery Time: 7-15 days
Payment Terms: T/T, L/C, D/A, Western Union
Supply Ability: TON
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 |
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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