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ALPHA,ALPHA,ALPHA'ALPHA'-TETRAMETHYL-1,3-BENZENEDIPROPIONITRILE, also known as BHT-CN, is a white, crystalline powder that is commonly used as a stabilizer and antioxidant in a variety of products. It is insoluble in water but soluble in organic solvents, making it suitable for use in various industries.

69774-36-3

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69774-36-3 Usage

Uses

Used in Plastics and Rubber Industry:
ALPHA,ALPHA,ALPHA'ALPHA'-TETRAMETHYL-1,3-BENZENEDIPROPIONITRILE is used as a stabilizer and antioxidant for plastics and rubbers to prevent degradation from heat, light, and oxygen exposure.
Used in Adhesives Industry:
ALPHA,ALPHA,ALPHA'ALPHA'-TETRAMETHYL-1,3-BENZENEDIPROPIONITRILE is used as a stabilizer and antioxidant in adhesives to enhance their durability and performance.
Used in Oils Industry:
ALPHA,ALPHA,ALPHA'ALPHA'-TETRAMETHYL-1,3-BENZENEDIPROPIONITRILE is used as a stabilizer and antioxidant in oils to extend their shelf life and maintain their quality.
Used in Food Packaging Industry:
ALPHA,ALPHA,ALPHA'ALPHA'-TETRAMETHYL-1,3-BENZENEDIPROPIONITRILE is used as a stabilizer and antioxidant in food packaging to extend the shelf life of food products and maintain their quality.
Used in Cosmetics and Personal Care Products Industry:
ALPHA,ALPHA,ALPHA'ALPHA'-TETRAMETHYL-1,3-BENZENEDIPROPIONITRILE is used as a stabilizer and antioxidant in cosmetics and personal care products to extend their shelf life and maintain their quality.
It is important to handle ALPHA,ALPHA,ALPHA'ALPHA'-TETRAMETHYL-1,3-BENZENEDIPROPIONITRILE with care due to its potential for skin and eye irritation, and it has been deemed safe for use in these applications by regulatory agencies.

Check Digit Verification of cas no

The CAS Registry Mumber 69774-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,7 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69774-36:
(7*6)+(6*9)+(5*7)+(4*7)+(3*4)+(2*3)+(1*6)=183
183 % 10 = 3
So 69774-36-3 is a valid CAS Registry Number.

69774-36-3Relevant academic research and scientific papers

Expanding the scope of C-H amination through catalyst design

Espino, Christine G.,Fiori, Kristin Williams,Kim, Mihyong,Du Bois

, p. 15378 - 15379 (2004)

Analysis of the mechanism for Rh-mediated C-H amination has led to the development of a remarkably effective dinuclear Rh catalyst derived from 1,3-benzenedipropionic acid. This unique complex, Rh2(esp)2, is capable of promoting both

Cobalt complexes of the chelating dicarboxylate ligand esp : A paddlewheel-type dimer and a heptanuclear coordination cluster

Pakula, Ryan J.,Berry, John F.

, p. 13887 - 13893 (2018)

The coordination chemistry of Co(ii) with the chelating dicarboxylate ligand esp (esp = α,α,α′,α′-tetramethyl-1,3-benzenedipropionate) is explored. We report here the bimetallic paddlewheel-type dimer, Co2(esp)2(EtOH)2 (1), and a bowl-shaped, heptanuclear coordination cluster, Co7(OH)4(Hesp)2(esp)4(MeCN)2·4MeCN (2). Crystal structures of both complexes are reported as well as their magnetic properties, which indicate antiferromagnetic interactions among the Co(ii) ions.

Observation of a Photogenerated Rh2 Nitrenoid Intermediate in C-H Amination

Das, Anuvab,Maher, Andrew G.,Telser, Joshua,Powers, David C.

supporting information, p. 10412 - 10415 (2018/08/28)

Rh2-catalyzed C-H amination is a powerful method for nitrogenating organic molecules. While Rh2 nitrenoids are often invoked as reactive intermediates in these reactions, the exquisite reactivity and fleeting lifetime of these species has precluded their observation. Here, we report the photogeneration of a transient Rh2 nitrenoid that participates in C-H amination. The developed approach to Rh2 nitrenoids, based on photochemical cleavage of N-Cl bonds in N-chloroamido ligands, has enabled characterization of a reactive Rh2 nitrenoid by mass spectrometry and transient absorption spectroscopy. We anticipate that photogeneration of metal nitrenoids will contribute to the development of C-H amination catalysis by providing tools to directly study the structures of these critical intermediates.

Bimetallic reductive elimination from dinuclear Pd(III) complexes

Powers, David C.,Benitez, Diego,Tkatchouk, Ekaterina,Goddard, William A.,Ritter, Tobias

supporting information; experimental part, p. 14092 - 14103 (2011/01/09)

In 2009, we reported C-halogen reductive elimination reactions from dinuclear Pd(III) complexes and implicated dinuclear intermediates in Pd(OAc)2-catalyzed C-H oxidation chemistry. Herein, we report results of a thorough experimental and theor

Conformational analysis by the ring current method. The structure of 2,2,13,13-tetramethyl[4.4]metacyclophane

Fukazawa, Yoshimasa,Usui, Shuji,Tanimoto, Koji,Hirai, Yoshimasa

, p. 8169 - 8175 (2007/10/02)

The conformational analysis of 2,2,13,13-tetramethyl[4.4]metacyclophane (4) using X-ray crystallographic analysis, molecular mechanics calculations, and the ring current method is presented. Compound 4 shows a characteristic temperature-dependent chemical

Bis(aminoneopentyl) aromatics

-

, (2008/06/13)

Aromatic-aliphatic diamines of the formula STR1 in which Ar is an arylene or substituted arylene are useful in preparing thermally stable, rigid, polyamides, polyureas and polyurethanes having a repeating unit of the formula STR2 in which Ar is arylene or substituted arylene, X is --NH-- or --O--, n is 0 or 1, and R is a divalent organic radical.

Bis(2-methyl-2-cyanopropyl) aromatics

-

, (2008/06/13)

Aromatic-aliphatic dinitriles of the formula STR1 in which Ar is an arylene or substituted arylene are useful in the preparation of the corresponding amines which are intermediates for the preparation of thermally stable, rigid, polyamides.

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