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2,2'-METHYLENEBIS(4-ETHYL-6-TERT-BUTYLPHENOL) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • China Largest Factory Manufacturer Supply High Quality 2,2′-Methylenebis(6-tert-butyl-4-ethylphenol);Antioxidant 425 CAS 88-24-4

    Cas No: 88-24-4

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  • 88-24-4 Structure
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    1. Product Name: 2,2'-METHYLENEBIS(4-ETHYL-6-TERT-BUTYLPHENOL)
    2. Synonyms: 2,2’-methylenebis(6-(1,1-dimethylethyl)-4-ethyl-pheno;2,2’-methylenebis(6-(1,1-dimethylethyl)-4-ethylphenol);2,2’-methylenebis(6-tert-butyl-4-ethyl-pheno;2,2’-methylenebis(ethyl-6-tert-butylphenol;2,2’-methylenebis[6-(1,1-dimethylethyl)-4-ethyl-pheno;2,2’-methylenebis[6-(1,1-dimethylethyl)-4-ethyl-Phenol;2,2'-Methylene-bis(4-ethyl-6-t-butyl) phenol;agidol7
    3. CAS NO:88-24-4
    4. Molecular Formula: C25H36O2
    5. Molecular Weight: 368.55
    6. EINECS: 201-814-0
    7. Product Categories: Diphenylmethanes (for High-Performance Polymer Research);Functional Materials;Reagent for High-Performance Polymer Research;Polymer Additives;Polymer Science;Stabilizers;Antiager
    8. Mol File: 88-24-4.mol
  • Chemical Properties

    1. Melting Point: 119-122 °C(lit.)
    2. Boiling Point: 458.86°C (rough estimate)
    3. Flash Point: 187.5 ºC
    4. Appearance: /
    5. Density: 1.010
    6. Vapor Pressure: 0Pa at 25℃
    7. Refractive Index: 1.4894 (estimate)
    8. Storage Temp.: Inert atmosphere,Room Temperature
    9. Solubility: Chloroform (Slightly), Methanol (Slightly)
    10. PKA: 11.37±0.48(Predicted)
    11. CAS DataBase Reference: 2,2'-METHYLENEBIS(4-ETHYL-6-TERT-BUTYLPHENOL)(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2,2'-METHYLENEBIS(4-ETHYL-6-TERT-BUTYLPHENOL)(88-24-4)
    13. EPA Substance Registry System: 2,2'-METHYLENEBIS(4-ETHYL-6-TERT-BUTYLPHENOL)(88-24-4)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. WGK Germany: 2
    5. RTECS: SL9800000
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 88-24-4(Hazardous Substances Data)

88-24-4 Usage

Uses

Antioxidant

Flammability and Explosibility

Notclassified

Safety Profile

Poison by intraperitoneal route. Experimental reproductive effects. When heated to decomposition it emits acrid smoke and irritating fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 88-24-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88-24:
(4*8)+(3*8)+(2*2)+(1*4)=64
64 % 10 = 4
So 88-24-4 is a valid CAS Registry Number.

88-24-4 Well-known Company Product Price

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  • Aldrich

  • (413143)  2,2′-Methylenebis(6-tert-butyl-4-ethylphenol)  

  • 88-24-4

  • 413143-100G

  • 936.00CNY

  • Detail

88-24-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Methylenebis(4-Ethyl-6-Tert-Butylphenol)

1.2 Other means of identification

Product number -
Other names 2-tert-butyl-6-[(3-tert-butyl-5-ethyl-2-hydroxyphenyl)methyl]-4-ethylphenol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88-24-4 SDS

88-24-4Synthetic route

formaldehyd
50-00-0

formaldehyd

6-di-t-butyl-4-ethylphenol
96-70-8

6-di-t-butyl-4-ethylphenol

2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)
88-24-4

2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)

Conditions
ConditionsYield
With hydrogenchloride
With potassium hydroxide
With sulfuric acid
2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)
88-24-4

2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)

C14H21IrO4*H2O

C14H21IrO4*H2O

C45H62Ir2O2

C45H62Ir2O2

Conditions
ConditionsYield
In toluene at 100℃; for 3h; Inert atmosphere; Schlenk technique;86%
2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)
88-24-4

2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)

titanium tetrachloride
7550-45-0

titanium tetrachloride

CH2(CH3CH2C(CH3)3C6H2O)2TiCl2
162583-17-7

CH2(CH3CH2C(CH3)3C6H2O)2TiCl2

Conditions
ConditionsYield
In diethyl ether (N2 or Ar); -30°C, stirring (2 h, 25°C); removing of the solvent, recrystn. (ether); elem. anal.;68%
2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)
88-24-4

2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)

tetrabenzyl titanium
17520-19-3

tetrabenzyl titanium

CH2(CH3CH2C(CH3)3C6H2O)2Ti(CH2C6H5)2

CH2(CH3CH2C(CH3)3C6H2O)2Ti(CH2C6H5)2

Conditions
ConditionsYield
In hexane (N2 or Ar); -40°C, stirring (2 h, 20°C); evapn. of the solvent, recrystn. (hexane, -40°C); elem. anal.;58%
2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)
88-24-4

2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)

titanium tetrachloride
7550-45-0

titanium tetrachloride

(CH2(CH3CH2C(CH3)3C6H2O)2)2Ti
162583-18-8

(CH2(CH3CH2C(CH3)3C6H2O)2)2Ti

Conditions
ConditionsYield
With NEt3 In diethyl ether (N2 or Ar); -40°C, stirring (20°C, 3 h), centrifugation; extn. (ether), removal of the solvent, recrystn. (hexane, -40°C);elem. anal.;50%
2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)
88-24-4

2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)

dimethylchloromethylphosphine oxide
1638-75-1

dimethylchloromethylphosphine oxide

2,2'-methylene-bis(6-tert-butyl-4-ethyl-1-dimethylphosphinylmethylenoxybenzene)
139605-08-6

2,2'-methylene-bis(6-tert-butyl-4-ethyl-1-dimethylphosphinylmethylenoxybenzene)

Conditions
ConditionsYield
With sodium hydroxide
With sodium 1) xylene, MeOH, 2) xylene, reflux, 8 h; Yield given. Multistep reaction;
titanium(IV) isopropylate
546-68-9

titanium(IV) isopropylate

2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)
88-24-4

2,2'-methylenebis-(4-ethyl-6-tert-butylphenol)

[Ti(OCH(CH3)2)2(CH2(C6H2(O)(C(CH3)3)(CH2CH3))2)]
936366-05-1

[Ti(OCH(CH3)2)2(CH2(C6H2(O)(C(CH3)3)(CH2CH3))2)]

Conditions
ConditionsYield
In toluene byproducts: isopropanol; complex obtained by react. of CH2(C6H2(OH)(t-Bu)Et)2 and Ti(OPri)4 in toluene at 60°C for 3 h; elem. anal.; complex washed with toluene and azeotropic distilated;

88-24-4Relevant articles and documents

METHODS AND COMPOSITIONS FOR INHIBITING VINYL AROMATIC MONOMER POLYMERIZATION

-

, (2013/03/26)

Methods and compositions are provided for inhibiting the polymerization of a vinyl aromatic monomer, such as styrene monomer, during elevated temperature processing thereof or during storage or shipment of polymer containing product. The compositions comprise a combination of a quinone methide derivative A) and a phenol compound B). The methods comprise adding from about 1-10,000 ppm of the combination to the monomer containing medium, per one million parts of the monomer.

COLOR DEVELOPING COMPOSITION CONTAINING MOLECULAR COMPOUND, AND RECORDING MATERIAL

-

, (2011/06/19)

Provided is a color-developing composition containing a molecular compound which has as a component compound a compound represented by formula (I) [wherein Y represents a C1-C12 hydrocarbon group which is chained or branched and saturated or unsaturated, or a C1-C8 hydrocarbon group which is chained or branched, saturated or unsaturated and has an ether or thioether bond; R1, R2, R3 and R4 each independently represent a C1-C6 alkyl group or C2-C6 alkenyl group; n, p, q and r each represents any integer of 0 to 4; and m represents any integer of 0 to 2]. Also provided is a recording material with a sufficient color-forming sensitivity, superior storage stability, and especially with an extremely little background fogging in a heat resistance test.

Thermosensitive recording material and color developer compound therefor

-

, (2008/06/13)

A thermosensitive recording material has a support and a thermosensitive coloring layer formed thereon containing a leuco dye and a color developer capable of inducing color formation in the leuco dye upon application of heat thereto, with the color developer including at least one compound (A) having in a molecule thereof at least two aromatic ring moieties with specific structures, selected from the group consisting of an aromatic ring moiety having at least one carboxyl group and electron-attracting functional group, an aromatic ring moiety having at least one carboxyl group and electron-donating functional group, and an aromatic ring moiety having at least one carboxyl group, free of the electron-attracting and electron-donating functional groups. An aromatic carboxylic acid compound serving as the above-mentioned compound (A) and the producing method thereof are also disclosed.

4-Formyl amino-n-methylpiperidine derivatives, the use thereof as stabilisers and organic material stabilised therewith

-

, (2008/06/13)

The present invention relates to 4-formylamino-N-methylpiperidine derivatives of the formula (I) where the variables are as defined in the Description, to a process for preparing these piperidine derivatives, to the use of these piperidine derivatives of the invention, or prepared according to the invention, for stabilizing organic material, in particular for stabilizing plastics or coating materials, and also to the use of these piperidine derivatives of the invention, or prepared according to the invention, as light stabilizers or stabilizers for wood surfaces. The present invention further relates to stabilized organic material which comprises these piperidine derivatives of the invention or prepared according to the invention.

Thioether substituted hydroxybenzophenones and stabilized compositions

-

, (2008/06/13)

2-Hydroxybenzophenone derivatives substituted in the 4′-position by a thioether moiety exhibit enhanced absorption in the UV at longer wavelength. Compositions comprising organic material subject to actinic degradation are beneficially stabilized with such derivatives.

Lubricant composition

-

, (2008/06/13)

A composition comprising a) a lubricant or a hydraulic fluid and b) at least one compound of the general formula I STR1 in which x=1 or 2 and, if x=1, R is as defined for R1 or R3 --O-- or, if x=2, R is as defined for R8, and R1 and R3 are, for example, alkyl, cycloalkyl, alkenyl, phenyl, naphthyl, aralkyl or alkaryl, or alkyl, cycloalkyl, alkenyl, phenyl, naphthyl, aralkyl or alkaryl, which are monosubstituted or polysubstituted by groups from the series comprising halogen, cyano, nitro, e.g. --OCH3 or e.g. --COOCH3, or alkyl, cycloalkyl, alkenyl, aralkyl or alkaryl which are interrupted by one or more groups from the series comprising --O--, --S--, --NH--, STR2 or alkyl, cycloalkyl, alkenyl, aralkyl or alkaryl which are monosubstituted or polysubstituted by groups from the series comprising halogen, cyano, nitro, e.g. --OCH3 or e.g. --COOCH3 and interrupted by one or more groups from the series comprising --O--, --S--, --NH--, STR3 and R2 is NR4 R5, --OR6 or --SR7, and R4 and R5 are identical or different and are, for example, --H, alkyl, phenyl, naphthyl, aralkyl or alkaryl, or R4 and R5, together with the N atom linking them, form, for example, a piperidine or morpholine radical, and R6 and R7 can be alkyl which may be interrupted by one or more groups from the series comprising --O--, --S--, --NH--, STR4 or are, for example, phenyl, naphthyl, alkaryl or aralkyl, and R8 can be alkylene which may be interrupted by at least one --O-- group or alkylidene which may be interrupted by at least one --O-- group. Some of the compounds of the formula I are novel. The compositions show an improved stability towards oxidative degradation, confer protection under extreme pressures and reduce frictional wear.

3,9-carbohydrate substituted 2,4,8,10-tetraoxa-3,9-diphosphaspiro(5.5)undecane phosphite stabilizers

-

, (2008/06/13)

Carbohydrate substituted phosphites of Formula I STR1 where A is a carbohydrate residue are effective stabilizers for polymers processed at elevated temperatures and subject to thermal or oxidative degradation.

Beta crystalline modification of 2,2',2"-nitrilo[triethyl-tris-(3,3',5,5'-tetra-tert-butyl-1,1'-biphenyl-2,2'-diyl) phosphite]

-

, (2008/06/13)

The beta crystalline modification of 2,2',2"-nitrilo[triethyl-tris-(3,3',5,5'-tetra-tert-butyl-1,1'-biphenyl-2,2'-diyl) phosphite] is obtained by crystallizing said compound from the melt at elevated temperatures. The beta crystalline form is an effective process stabilizer for polyolefins, particularly polypropylene.

Substituted 1,4-diamino-2-butene stabilizers

-

, (2008/06/13)

N,N,N',N'-Tetrasubstituted 1,4-diamino-2-butenes where the substituents are alkyl, cycloalkyl, aralkyl, aryl or mixtures thereof provide effective antioxidant protection to lubricants and/or synthetic polymers.

Perfluoroalkyl substituted hydroxyphenylalkanoic ester antioxidants and stabilized compositions

-

, (2008/06/13)

Perfluoroalkyl substituted neopentyl alcohols can be reacted with substituted hydroxphenylalkanoic esters to form perfluoroalkyl containing hydroxyphenylalkanoic ester antioxidants. The perfluoroalkyl substituted hindered hydroxyphenyl alkanoates are stablizers which confer superior processing stability to polymers processed at elevated temperatures such as polypropylene, as well as protecting said polymers from thermal and oxidative degradation.

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