What is the p-Cumylphenol?

p-Cumylphenol is cream solid, while it's Molecular Formula is C15H16O. cream solid Used in Plastic and Rubber Industries: p-Cumylphenol is used as an intermediate for the production of antioxidants, stabilizers, and UV absorbers. Its presence in these additives helps to prevent the degradation of plastics and rubbers, thereby enhancing their durability and performance. Used in Pharmaceutical Industry: p-Cumylphenol serves as an intermediate in the production of pharmaceuticals. Its unique chemical structure contributes to the development of various medicinal compounds, making it an essential component in the pharmaceutical manufacturing process. Used in Disinfectant Production: Due to its antimicrobial properties, p-Cumylphenol is used as an intermediate in the production of disinfectants. It helps to eliminate harmful microorganisms, ensuring cleanliness and safety in various applications. Used in Fragrance Industry: p-Cumylphenol is employed as an intermediate in the production of fragrances. Its unique scent profile contributes to the creation of various fragrances used in personal care and cosmetic products. Used in Personal Care and Cosmetic Products: Leveraging its antimicrobial properties, p-Cumylphenol is used in personal care and cosmetic products to maintain cleanliness and prevent the growth of harmful microorganisms. It helps to ensure the safety and efficacy of these products. However, it is important to note that prolonged or repeated exposure to p-Cumylphenol may cause skin or eye irritation. Therefore, proper safety measures should be taken when handling p-Cumylphenol.

What is the CAS number for p-Cumylphenol?

The CAS number of p-Cumylphenol is 599-64-4.

What is p-Cumylphenol (599-64-4) used for?

p-Cumylphenol, also known as 4-Isopropylphenol, is a chemical compound belonging to the phenol group. It is a white solid with a faint odor and is soluble in organic solvents such as ethanol and ether. This versatile compound is widely used as an intermediate in various industries due to its unique properties.InChI:InChI=1/C15H16O/c1-12(11-13-5-3-2-4-6-13)14-7-9-15(16)10-8-14/h2-10,12,16H,11H2,1H3

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P-cumylphenol

CasNo599-64-4
Molecular FormulaC₁₅H₁₆O
Molecular Weight212.291
Purity
Appearancecream solid
Packing
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Molecular Formula:C15H16O
Molecular Weight:212.291
Appearance/Colour:cream solid
Vapor Pressure:0.000207mmHg at 25°C
Melting Point:72-75 °C
Refractive Index:1.587
Boiling Point:338.5 °C at 760 mmHg
Flash Point:160.5 °C
PSA：20.23000
Density:1.055 g/cm³
LogP:3.71810

p-Cumylphenol(Cas 599-64-4) Usage

General Description

p-Cumylphenol, also known as 4-Isopropylphenol, is a chemical compound that belongs to the group of phenols. It is a white solid with a faint odor and is soluble in organic solvents such as ethanol and ether. p-Cumylphenol is commonly used as an intermediate in the production of antioxidants, stabilizers, and UV absorbers in the plastic and rubber industries. It is also employed as an intermediate in the production of pharmaceuticals, disinfectants, and fragrances. Additionally, p-Cumylphenol is known to have antimicrobial properties and is used in various personal care and cosmetic products. However, prolonged or repeated exposure to p-Cumylphenol may cause skin or eye irritation, and it should be handled with proper safety measures.

InChI:InChI=1/C15H16O/c1-12(11-13-5-3-2-4-6-13)14-7-9-15(16)10-8-14/h2-10,12,16H,11H2,1H3

599-64-4 Relevant articles

MULTISTEP PROCESS FOR THE PREPARATION OF HEXAMETHYLENE DIISOCYANATE, PENTAMETHYLENE DIISOCYANATE OR TOLUENE DIISOCYANATE

-

Page/Page column 11, (2019/04/26)

The present invention relates to a multi...

Catalytic Hydroarylation of Alkenes with Phenols using B(C6F5)3

Bentley, Jordan N.,Caputo, Christopher B.

supporting information, p. 3654 - 3658 (2018/10/20)

We demonstrate that tris(pentafluorophen...

METHOD FOR MANUFACTURING α-METHYLSTYRENATED PHENOL

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Paragraph 0035; 0036; 0072; 0073; 0076; 0084, (2017/10/14)

According to an embodiment of the presen...

Phenylethyl/heteroploid c phenyl phenol preparation method of compound (by machine translation)

-

Paragraph 0017; 0018; 0019; 0020; 0021; 0022; 0023, (2016/10/17)

The invention relates to phenyl-based/he...

599-64-4 Process route

: 98-83-9,6144-04-3,25014-31-7,42612-14-6
isopropenylbenzene

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

: 599-64-4
p-cumylphenol

: 2772-45-4,106060-52-0
2,4-di-cumylphenol

Conditions

Conditions	Yield
With decacarbonyldirhenium⁽⁰⁾; In toluene; at 150 ℃; for 24h; regioselective reaction; Inert atmosphere; Sealed tube;	86% 8%

: 98-83-9,6144-04-3,25014-31-7,42612-14-6
isopropenylbenzene

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

: 599-64-4
p-cumylphenol

: 3910-35-8
1,1,3-trimethyl-3-phenylindane

: 2772-45-4,106060-52-0
2,4-di-cumylphenol

: 6362-80-7
2,4-diphenyl-4-methyl-pent-1-ene

: 22768-22-5,22768-23-6,6258-73-7
4-methyl-2,4-diphenylpent-2-ene

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate; at 90 - 100 ℃; for 4.33333h; Temperature;	16.15 %Chromat. 16.03 %Chromat. 40.74 %Chromat.

599-64-4 Upstream products

98-82-8
Isopropylbenzene
617-94-7
1-methyl-1-phenylethyl alcohol
80-15-9
Cumene hydroperoxide
6623-93-4
1-(2-(4-methoxyphenyl)propan-2-yl)benzene

599-64-4 Downstream products

3692-16-8
4-(1-methyl-1-phenyl-ethyl)-2,6-bis-piperidinomethyl-phenol
116281-64-2
2,6-bis-[2-hydroxy-5-(1-methyl-1-phenyl-ethyl)-benzyl]-4-methyl-phenol
24133-64-0
4-(1-methyl-1-phenyl-ethyl)-2-nitro-phenol
22223-51-4
2,6-dichloro-4-(1-methyl-1-phenyl-ethyl)-phenol