1817-68-1

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• Basic information

  1. Product Name: 2,6-bis(1-phenylethyl)-p-cresol
  2. Synonyms: 2,6-bis(1-phenylethyl)-p-cresol;2,6-bis(1-phenylethyl)-4-methylphenol;2,6-bis(alpha-methylbenzyl)-p-creso;4-Methyl-2,6-bis(1-phenylethyl)phenol;ALKYLATED P-CRESOL;2,6-Bis-(ALPHA-methylbenzyl)-p-cresol;4-Methyl-2,6-bis(α-methylbenzyl)phenol;Alcofen MBP
  3. CAS NO:1817-68-1
  4. Molecular Formula: C₂₃H₂₄O
  5. Molecular Weight: 316.43606
  6. EINECS: 217-328-7
  7. Product Categories: N/A
  8. Mol File: 1817-68-1.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 415.85°C (rough estimate)
  3. Flash Point: 203.9°C
  4. Appearance: /
  5. Density: 1.0031 (rough estimate)
  6. Vapor Pressure: 3.05E-08mmHg at 25°C
  7. Refractive Index: 1.6380 (estimate)
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 2,6-bis(1-phenylethyl)-p-cresol(CAS DataBase Reference)
  11. NIST Chemistry Reference: 2,6-bis(1-phenylethyl)-p-cresol(1817-68-1)
  12. EPA Substance Registry System: 2,6-bis(1-phenylethyl)-p-cresol(1817-68-1)

• 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: 1817-68-1(Hazardous Substances Data)

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• SDS
• Upstream product
• Downstream Products
• Article

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• 2,6-bis(1-phenylethyl)-p-cresol

  Cas No: 1817-68-1

• USD $ 3.0-3.0 / Kilogram

• 1 Kilogram

• 1-100 Metric Ton/Month

• Dayang Chem (Hangzhou) Co.,Ltd.
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• Pharmaceutical Grade CAS 1817-68-1 with competitive price

  Cas No: 1817-68-1

• USD $ 139.0-210.0 / Kilogram

• 1 Kilogram

• 1000 Kilogram/Day

• Zhuozhou Wenxi import and Export Co., Ltd
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• Phenol,4-methyl-2,6-bis(1-phenylethyl)-

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• Hangzhou J&H Chemical Co., Ltd.
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• Phenol,4-methyl-2,6-bis(1-phenylethyl)-

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• 10 Gram

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• Zibo Hangyu Biotechnology Development Co., Ltd
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• Phenol,4-methyl-2,6-bis(1-phenylethyl)-

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• 2,6-BIS(A-METHYLBENZYL)-P-CRESOL

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• Hangzhou Fandachem Co.,Ltd
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• Phenol,4-methyl-2,6-bis(1-phenylethyl)-

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• Chemlyte Solutions
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• 2,6-bis(1-phenylethyl)-p-cresol

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• Shanghai Run-Biotech Co., Ltd.
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• CSR201608-4252

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• Skyrun Industrial Co.,Ltd
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1817-68-1 Usage

General Description

2,6-bis(1-phenylethyl)-p-cresol, also known as BPEPC, is a chemical compound commonly used as an antioxidant in polymers and plastic materials. It is a white to pale yellow solid with a molecular formula C28H30O and a molecular weight of 394.54 g/mol. BPEPC is a highly effective antioxidant, able to inhibit the oxidation of materials by scavenging free radicals and preventing the degradation of polymers due to exposure to heat, light, or oxygen. It is also used in the manufacturing of rubber products, adhesives, lubricants, and coatings to improve their stability and durability. However, BPEPC has been identified as a potential endocrine disruptor and may have adverse effects on human health and the environment, leading to restrictions on its use in certain applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1817-68-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,1 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1817-68:
(6*1)+(5*8)+(4*1)+(3*7)+(2*6)+(1*8)=91
91 % 10 = 1
So 1817-68-1 is a valid CAS Registry Number.

InChI:InChI=1/C23H24O/c1-16-14-21(17(2)19-10-6-4-7-11-19)23(24)22(15-16)18(3)20-12-8-5-9-13-20/h4-15,17-18,24H,1-3H3

1817-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-methyl-2,6-bis(1-phenylethyl)phenol

1.2 Other means of identification

Product number	-
Other names	Alkofen MBP

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:1817-68-1 SDS

1817-68-1Upstream product

• 100-42-5 styrene 
• 106-44-5 p-cresol 

1817-68-1Downstream Products

1817-68-1Relevant articles and documents

Catalytic synthesis of 4-methyl-2-(α-methyl benzyl) phenol over fe-al-mcm-41 for extraction-separation rubidium from brine

Feng, Zhenhua,An, Lianying,Huang, Zhenggen,Zhao, Xianyin,Wang, Bengao

, p. 141 - 147 (2021/02/05)

A new extractant 4-methyl-2-(α-methyl benzyl) phenol had been synthesized with styrene and p-cresol through the Friedel-Crafts alkylation reaction. Fe-Al-MCM-41 which was used as molecular sieves catalyst for the synthesis of the extractant was prepared by hydrothermal synthesis method and then characterized by FT-IR, XRD, NH3-TPD and N2 adsorption isotherm. The catalytic synthesis conditions of 4-methyl-2-(α-methyl benzyl) phenol such as reaction time, temperature and catalyst dosage were investigated. The conversion of styrene was about 81.2%, the target product yield and selectivity can reach 74.6% and 95.7% respectively. The structure of the 4-methyl-2-(α-methyl benzyl) phenol was confirmed by 1H-NMR. At the same time, 4-methyl-2-(α-methyl benzyl) phenol was used as extractant to separate rubidium from brine of which the rate of potassium to rubidium is 10:1 (CK+=10.0g/L, CRb+=1.0g/L). The experiment results show that the extractant has a great extraction performance to rubidium, the extraction yields of rubidium and potassium can reach 81.1% and 9.4% respectively. The separation factor of Rb+/K+ can reach up to 41.4.

REACTION OF o-, m-, AND p-CRESOL WITH STYRENE IN THE PRESENCE OF ALUMINIUM CRESOLATES

Kozlikovskii, Ya. B.,Chernyaev, B. V.,Litvin, A. L.,Kofanova, A. V.

, p. 1325 - 1330 (2007/10/02)

The alkylation of o-, m-, and p-cresol by styrene in the presence of aluminium cresolates gives a mixture of isomeric (α-methylbenzyl)cresols, whose composition is predominated by the ortho-alkylation products. 2,6-Di(α-methylbenzyl)-4-methylphenol has been separated into a racemate and the meso form, whose ratio varies from 1:1 (130 deg C) to 2:1 (210 deg C).The erythro and threo forms of 2,6-di(α-methylbenzyl)-3-methylphenol have been recovered in ratios equal to 1:1.4 (130 deg C) and 1:1.29 (150 deg C), which point out the stereospecifity of the alkylation reaction.

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