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o-(1,1,3,3-tetramethylbutyl)phenol, also known as BHT or butylated hydroxytoluene, is a synthetic organic compound widely used as an antioxidant and preservative in various industries. It is a white crystalline solid with a molecular formula of C15H24O and a molecular weight of 220.35 g/mol. BHT is effective in preventing the oxidation of fats and oils, making it a common additive in food products, cosmetics, and pharmaceuticals. It also has applications in rubber, petroleum, and chemical manufacturing to protect against oxidative degradation. Despite its benefits, BHT has been a subject of debate due to potential health concerns, and its use is regulated in different countries.

3884-95-5

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3884-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3884-95-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,8 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3884-95:
(6*3)+(5*8)+(4*8)+(3*4)+(2*9)+(1*5)=125
125 % 10 = 5
So 3884-95-5 is a valid CAS Registry Number.
InChI:InChI=1S/C14H22O/c1-13(2,3)10-14(4,5)11-8-6-7-9-12(11)15/h6-9,15H,10H2,1-5H3

3884-95-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,4,4-trimethylpentan-2-yl)phenol

1.2 Other means of identification

Product number -
Other names 2-tert-octylphenol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Oxidizing/reducing agents
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:3884-95-5 SDS

3884-95-5Relevant academic research and scientific papers

ALKYLATION OF HYDROXYARENES WITH OLEFINS, ALCOHOLS AND ETHERS IN IONIC LIQUIDS

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Page/Page column 16-17, (2008/06/13)

Hydroxyarenes are alkylated using an ionic liquid catalyst system with olefins, alcohols, or ethers as alkylating agents. The ionic liquid catalyst system comprises chloroindate (III) anions. The reactions may be conducted at moderate temperatures and pressures to yield commercially relevant alkylated hydroxyarene compounds.

Synthesis of 4-tert-octylphenol and 4-cumylphenol by metal triflate and metal triflimidate catalysts

Le Rouzo, Guillaume,Morel-Grepet, Marielle,Simonato, Jean-Pierre

, p. 521 - 522 (2007/10/03)

Metal inflates and metal triflimidates are shown to catalyse efficiently the Friedel-Crafts alkylation of phenol with alkenes. Bismuth, copper and scandium triflates lead to very good yields with excellent para-selectivities.

The separation and synthesis of lipidic 1,2- and 1,3-diols from natural phenolic lipids for the complexation and recovery of boron

Tyman, John H.P.,Mehet, Satinderjit K.

, p. 177 - 199 (2007/10/03)

A study has been made of the semi-synthesis of 1,3-diols (anacardic alcohols) from natural phenolic lipid resources from Anacardium occidentale and Anacardium giganteum which have given C15 and C11 derivatives, respectively. An isomeric 1,3-diol (isoanacardic alcohol) has been obtained from cardanol separated from technical cashew nut-shell liquid. Homologous1,3-diols have been synthesised from a range of synthetic 2-alkyl-, 3-alkyl- and 4-alkylphenols and from 6-alkylsalicylic acids. The natural 1,2-diol, urushiol, from Rhus vernicifera has been purified. All these lipidic compounds have been studied for their complexation and the potential recovery of boron as boric acid.

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