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2,4-DIHYDROXY-1,3,5-TRIMETHYLBENZENE

Base Information Edit
  • Chemical Name:2,4-DIHYDROXY-1,3,5-TRIMETHYLBENZENE
  • CAS No.:608-98-0
  • Molecular Formula:C9H12 O2
  • Molecular Weight:152.193
  • Hs Code.:2907299090
  • Mol file:608-98-0.mol
2,4-DIHYDROXY-1,3,5-TRIMETHYLBENZENE

Synonyms:Mesorcinol(6CI); Resorcinol, 2,4,6-trimethyl- (7CI,8CI); 2,4-Mesitylenediol; Mesorcin;NSC 52676

Suppliers and Price of 2,4-DIHYDROXY-1,3,5-TRIMETHYLBENZENE
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 2,4-Dihydroxy-1,3,5-trimethylbenzene
  • 200mg
  • $ 175.00
  • Biosynth Carbosynth
  • 2,4-Dihydroxy-1,3,5-trimethylbenzene
  • 1 g
  • $ 150.00
  • Biosynth Carbosynth
  • 2,4-Dihydroxy-1,3,5-trimethylbenzene
  • 500 mg
  • $ 90.00
  • Biosynth Carbosynth
  • 2,4-Dihydroxy-1,3,5-trimethylbenzene
  • 250 mg
  • $ 50.00
  • Biosynth Carbosynth
  • 2,4-Dihydroxy-1,3,5-trimethylbenzene
  • 2 g
  • $ 250.00
  • American Custom Chemicals Corporation
  • 2,4,6-TRIMETHYLBENZENE-1,3-DIOL 95.00%
  • 5MG
  • $ 496.82
Total 6 raw suppliers
Chemical Property of 2,4-DIHYDROXY-1,3,5-TRIMETHYLBENZENE Edit
Chemical Property:
  • Melting Point:150.8°C 
  • Refractive Index:1.4024 (estimate) 
  • Boiling Point:274.5°C (estimate) 
  • PSA:40.46000 
  • Density:0.967g/cm3 
  • LogP:2.02300 
Purity/Quality:

98%min *data from raw suppliers

2,4-Dihydroxy-1,3,5-trimethylbenzene *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 2,4-DIHYDROXY-1,3,5-TRIMETHYLBENZENE

There total 15 articles about 2,4-DIHYDROXY-1,3,5-TRIMETHYLBENZENE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 3 steps
1: aq. NH3, H2S / ethanol / Heating
2: (i) aq. H2SO4, NaNO2, (ii) (heating)
3: (i) Sn, aq. HCl, (ii) NaNO2, aq. H2SO4, (iii) (heating)
With ammonium hydroxide; hydrogen sulfide; In ethanol;
DOI:10.1139/v65-200
Guidance literature:
Multi-step reaction with 4 steps
1: HNO3
2: aq. NH3, H2S / ethanol / Heating
3: (i) aq. H2SO4, NaNO2, (ii) (heating)
4: (i) Sn, aq. HCl, (ii) NaNO2, aq. H2SO4, (iii) (heating)
With ammonium hydroxide; hydrogen sulfide; nitric acid; In ethanol;
DOI:10.1139/v65-200
Guidance literature:
Multi-step reaction with 2 steps
1: H2O / diethyl ether
2: aq. HCl / Heating
With hydrogenchloride; water; In diethyl ether;
DOI:10.1039/jr9600000001
Refernces Edit
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