1,1,3-Tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane

Base Information

• Chemical Name: 1,1,3-Tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane
• CAS No.: 1843-03-4
• Deprecated CAS: 111214-48-3,134685-22-6,134707-88-3,27322-35-6,82278-68-0,125052-71-3,134685-22-6,134707-88-3,27322-35-6,82278-68-0
• Molecular Formula: C37H52O3
• Molecular Weight: 544.818
• Hs Code.: 2907199090
• European Community (EC) Number: 217-420-7
• UNII: BF6E9O0XJN
• DSSTox Substance ID: DTXSID0038883
• Nikkaji Number: J47.628E
• Wikidata: Q27274633
• RXCUI: 1872247
• Mol file: 1843-03-4.mol

Synonyms:1843-03-4;Topanol CA;1,1,3-Tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane;Trisalkofen BMB;Topanol SA;TPNC;Tri(butylcresyl)butane;GSY 930;MARK AO 30;1,1,3-Tris(5-tert-butyl-4-hydroxy-2-methylphenyl)butane;EINECS 217-420-7;UNII-BF6E9O0XJN;BF6E9O0XJN;BRN 2318488;4,4',4''-(1-Methylpropanyl-3-ylidene)tris(6-tert-butyl-m-cresol);4,4',4''-(1-Methylpropanyl-3-ylidene)tris[6-tert-butyl-m-cresol];4,4',4''-(Butane-1,1,3-triyl)tris(2-(tert-butyl)-5-methylphenol);OS-930;4-[4,4-bis(5-tert-butyl-4-hydroxy-2-methylphenyl)butan-2-yl]-2-tert-butyl-5-methylphenol;Phenol, 4,4',4''-(1-methyl-1-propanyl-3-ylidene)tris(2-(1,1-dimethylethyl)-5-methyl-;39283-48-2;1,1,3-tri(3-tert-butyl-4-hydroxy-6-methylphenyl)butane;EC 217-420-7;4,4',4''-(1-Methyl-1-propanyl-3-ylidene)tris(2-(1,1-dimethylethyl)-5-methylphenol);4,4',4''-(1-Methyl-1-propanyl-3-ylidene)tris(2-(1,1-dimethylethyl- )-5-methylphnol);1,3-Tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane;m-Cresol, 4,4',4''-(1-methyl-1-propanyl-3-ylidene)tris(6-tert-butyl-;Phenol, 4,4',4''-(3-methylpropane-1,1,3-triyl)tris(2-tert-butyl-5-methyl-;C37-H52-O3;Phenol, 4,4',4''-(1-methyl-1-propanyl-3-ylidene)tris 2-(1,1-dimethylethyl)-5-methyl-;Phenol, 4,4',4''-(1-methyl-1-propanyl-3-ylidene)tris(2-(1,1-dimethylethyl- )-5-methyl-;Phenol, 4,4',4''-(1-methyl-1-propanyl-3-ylidene)tris[2-(1,1-dimethylethyl)-5-methyl-;m-Cresol, 4,4',4''-(1-methyl-1-propanyl-3-ylidene)tris[6-tert-butyl-;Lowinox CA 22;ANTIOXIDANT CA;4,4',4''-butane-1,1,3-triyltris(2-tert-butyl-5-methylphenol);Phenol, 4,4',4''-(1-methyl-1-propanyl- 3-ylidene)tris[2-(1,1-dimethylethyl)-5-methyl -;SCHEMBL26591;DTXSID0038883;BP_23;C37H52O3;MFCD00072238;AKOS025294776;AS-84192;LS-104930;LS-104931;FT-0774975;E77749;W-109717;Q27274633;1,1,3-tris(2-methyl-4-hydroxy-5-t-butylphenyl)butane;1,1,3-tris(2'-methyl-4'-hydroxy-5'-t-butylphenyl)butane;1,1,3-Tris-(2-methyl-4-hydroxy-5-t-butylphenyl) butane;1,1,3-tris-(4-hydroxy-2-methyl-5-t-butylphenyl) butane;1,1,3-tris(2'-methyl-4'-hydroxy -5'-t-butylphenyl) butane;1,1,3-Tris(2-methyl-4-hydroxy-5-t-butylphenyl)butane, 99%;4,4',4''-(Butane-1,1,3-triyl)tris(2-tert-butyl-5-methylphenol);4, 4', 4''- (1- methylpropanyl- 3- ylidene)tris[6- tert- butyl- m- cresol];4,4',4''-(1-METHYLPROPANYL-3-YLIDENE)TRIS(6-TERT-BUTYL-M- CRESOL);m-Cresol, 4,4',4''-(1-methyl-1-propanyl-3-ylidene)tris(6-tert-butyl- (7CI,8CI);1,1,3-Tris(2 inverted exclamation mark -methyl-4 inverted exclamation mark -hydroxy-5 inverted exclamation mark -t- butylphenyl)butane;4,4',4''-(1-METHYL-1-PROPANYL-3-YLIDENE)TRIS(2-(1,1- DIMETHYLETHYL- )-5-METHYLPHNOL)

Chemical Property of 1,1,3-Tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane

Chemical Property:

• Appearance/Colour: off-white to tan Crystalline powder
• Vapor Pressure: 1.91E-15mmHg at 25°C
• Melting Point: 183-190 °C(lit.)
• Refractive Index: 1.558
• Boiling Point: 609.416 °C at 760 mmHg
• PKA: 10.38±0.20(Predicted)
• Flash Point: 233.376 °C
• PSA: 60.69000
• Density: 1.038 g/cm³
• LogP: 9.94680
• Water Solubility.: 0.02ng/L at 20℃
• XLogP3: 11.5
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 8
• Exact Mass: 544.39164552
• Heavy Atom Count: 40
• Complexity: 758

Purity/Quality:

99% ^*data from raw suppliers

1,1,3-TRIS-(2-TERT-BUTYL-4-HYDROXY-5-METHYLPHENYL)BUTANE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC(=C(C=C1C(C)CC(C2=CC(=C(C=C2C)O)C(C)(C)C)C3=CC(=C(C=C3C)O)C(C)(C)C)C(C)(C)C)O
• Uses: 1,1,3-Tris(2-Methyl-4-hydroxy-5-tert-butylphenyl)butane is an excellent phenolic antioxidant and can be used as a stabilizer in polypropylene, polyethylene, polyvinyl chloride, ABS, polyoxymethylene and other resins and light-colored rubber products. It works synergistically with the antioxidant DLTP.

Technology Process of 1,1,3-Tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane

There total 1 articles about 1,1,3-Tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane 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:

Reference yield:

→ 1,1,3-tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane (1843-03-4)

Guidance literature:

Reference yield: 86.0%

2,2,6,6-Tetramethyl-1-piperidinyloxy free radical (2564-83-2,45842-10-2,126517-51-9,25657-03-8,26933-82-4,54637-06-8,64104-42-3) + 1,1,3-tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane (1843-03-4) → C37H52O3*3C9H18NO

Guidance literature:

In toluene;

DOI:10.1021/ja015849+

Reference yield: 70.0%

(E)-3-[4-[6-(2-methylprop-2-enoyloxy)hexoxy]phenyl]prop-2-enoic acid (125274-23-9) + 1,1,3-tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane (1843-03-4) → CLM_007

Guidance literature:

With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 24h;

Downstream raw materials:

1,1,3-tris(5'-tert-butyl-2'-methyl-4'-dimethylphosphinylmethyleneoxybenzene)butane

C₄₀H₅₂O₆

Refernces

• 1、 -. "4-Formyl amino-n-methylpiperidine derivatives, the use thereof as stabilisers and organic material stabilised therewith". . . Retrieved 2008/06/13.
• 2、 -. "4-acylaminopiperidin-N-oxyle". . . Retrieved 2008/06/13.