4-Pentylphenol

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China cas 14938-35-3 factory wholesale 4-Pentylphenol at affordable price

  • Molecular Formula: C11H16O
  • Molecular Weight: 164.247
  • Appearance/Colour: clear light yellow to light brown liquid 
  • Melting Point: 23-25 °C 
  • Refractive Index: n20/D 1.515  
  • Boiling Point: 250.5 °C at 760 mmHg 
  • PKA: 10.26±0.13(Predicted) 
  • Flash Point: 135 °C 
  • PSA: 20.23000 
  • Density: 0.964 g/cm3 
  • LogP: 3.12490 

4-Pentylphenol(Cas 14938-35-3) Usage

Synthesis Reference(s)

Tetrahedron Letters, 19, p. 2545, 1978 DOI: 10.1016/S0040-4039(01)94822-1

Safety Profile

Questionable carcinogen with experimental neoplas tigenic data. Moderately flammable. To fight fire, use foam, Co2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes.

InChI:InChI=1/C11H16O/c1-2-3-4-5-10-6-8-11(12)9-7-10/h6-9,12H,2-5H2,1H3

14938-35-3 Relevant articles

C70 Fullerene-Catalyzed Metal-Free Photocatalytic ipso-Hydroxylation of Aryl Boronic Acids: Synthesis of Phenols

Kumar, Inder,Sharma, Ritika,Kumar, Rakesh,Kumar, Rakesh,Sharma, Upendra

supporting information, p. 2013 - 2019 (2018/04/02)

A metal-free C70 fullerene-catalyzed met...

Pd-Catalyzed Hydroxylation of Aryl Boronic Acids Using In Situ Generated Hydrogen Peroxide

Yi, Hong,Lei, Aiwen

supporting information, p. 10023 - 10027 (2017/08/01)

Herein, we describe a benign and efficie...

POLAR NEMATIC COMPOUNDS

-

, (2011/06/28)

Polar nematic compounds, one example of ...

Synthesis and Antimicrobial Activity of Hydroxyalkyl- and Hydroxyacyl-phenols and Their Benzyl Ethers

Krauss, J.,Unterreitmeier, D.

, p. 94 - 98 (2007/10/03)

New phenolic compounds with hydrophilic ...

14938-35-3 Process route

1-bromo-butane
109-65-9

1-bromo-butane

p-cresol
106-44-5

p-cresol

4-n-pentylphenol
14938-35-3

4-n-pentylphenol

2-Butyl-4-methylphenol
6891-45-8

2-Butyl-4-methylphenol

4,4'-ethylenediphenol
6052-84-2

4,4'-ethylenediphenol

4-pentylbutoxybenzene
101144-97-2

4-pentylbutoxybenzene

Conditions
Conditions Yield
With n-butyllithium; potassium tert-butylate; Yield given. Multistep reaction. Further byproducts given. Yields of byproduct given; 1.) heptane, hexane, reflux, 20 h, 2.) THF;
pentanal
110-62-3

pentanal

phenol
108-95-2,27073-41-2

phenol

4-n-pentylphenol
14938-35-3

4-n-pentylphenol

2-pentylphenol
136-81-2

2-pentylphenol

1,1-Bis(4-hydroxyphenyl)pentane
17181-62-3

1,1-Bis(4-hydroxyphenyl)pentane

C<sub>17</sub>H<sub>20</sub>O<sub>2</sub>

C17 H20 O2

Conditions
Conditions Yield
With Al(3+)-montmorillonite; at 100 ℃; for 48h; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;

14938-35-3 Upstream products

  • 110-62-3
    110-62-3

    pentanal

  • 108-95-2
    108-95-2

    phenol

  • 109-65-9
    109-65-9

    1-bromo-butane

  • 106-44-5
    106-44-5

    p-cresol

14938-35-3 Downstream products

  • 18980-03-5
    18980-03-5

    2-chloro-4-pentylphenol

  • 408328-48-3
    408328-48-3

    3-Nitro-4-hydroxy-1-pentyl-benzol

  • 64191-92-0
    64191-92-0

    benzoic acid-(4-pentyl-phenyl ester)

  • 4099-75-6
    4099-75-6

    2,6-dinitro-4-pentyl-phenol

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