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132610-60-7

2-(1-Butyl-octyl)-phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132610-60-7 Structure

  • Basic information

    1. Product Name: 2-(1-Butyl-octyl)-phenol
    2. Synonyms:
    3. CAS NO:132610-60-7
    4. Molecular Formula:
    5. Molecular Weight: 262.436
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132610-60-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(1-Butyl-octyl)-phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(1-Butyl-octyl)-phenol(132610-60-7)
    11. EPA Substance Registry System: 2-(1-Butyl-octyl)-phenol(132610-60-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 132610-60-7(Hazardous Substances Data)

132610-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132610-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,6,1 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132610-60:
(8*1)+(7*3)+(6*2)+(5*6)+(4*1)+(3*0)+(2*6)+(1*0)=87
87 % 10 = 7
So 132610-60-7 is a valid CAS Registry Number.

132610-60-7Downstream Products

132610-60-7Relevant articles and documents

Alkylation of Phenol by 1-Dodecene and 1-Decanol. A Literature Correction

Campbell, Curt B.,Onopchenko, Anatoli,Santilli, Donald S.

, p. 3665 - 3669 (1990)

A recent literature report that 1-dodecene reacts with phenol in the presence of sulfated zirconium oxide (superacid), or 1-dodecanol with phenol in the presence of H-Mordenite (zeolite), to afford mostly para-substituted alkylphenols has been shown to be incorrect.The product with zirconium is a mixture of ortho/para isomers (ca. 50-65/50-35), and not the exclusive para isomer as reported.The major product in the case of zeolite catalysis is the o-alkylphenol, with a high degree of end attachment, and not the predominantly claimed para isomers.The selectivity obtained with H-Mordenite during alkylation of phenol differs from the a lkylation of alkylbenzenes and anisole, and is best explained on the basis of a surface catalysis phenomenon.

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