1643-39-6

Basic information

• Product Name: 2-AMINO-4,6-DI-TERT-BUTYLPHENOL
• Synonyms: 2-AMINO-4,6-DI-TERT-BUTYLPHENOL;4,6-Di-tert-butyl-2-aminophenol;2-AMino-4,6-di-tert.-butyl-phenoxyl
• CAS NO: 1643-39-6
• Molecular Formula: C₁₄H₂₃NO
• Molecular Weight: 221.34
• Mol File: 1643-39-6.mol
• Article Data: 29

Chemical Properties

• Melting Point: 171-172 °C
• Boiling Point: 297.9±40.0 °C(Predicted)
• Appearance: /
• Density: 0.990±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 11.36±0.23(Predicted)
• CAS DataBase Reference: 2-AMINO-4,6-DI-TERT-BUTYLPHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-4,6-DI-TERT-BUTYLPHENOL(1643-39-6)
• EPA Substance Registry System: 2-AMINO-4,6-DI-TERT-BUTYLPHENOL(1643-39-6)

Safety Data

• Hazardous Substances Data: 1643-39-6(Hazardous Substances Data)

Usage

General Description

2-AMINO-4,6-DI-TERT-BUTYLPHENOL is a chemical compound with the molecular formula C14H23NO. It is commonly used as an antioxidant in various industrial applications, including in the production of polymers and plastics. The compound is a white crystalline solid at room temperature and is insoluble in water. It is known for its ability to inhibit the oxidation of other substances, making it a valuable additive in products where stability and shelf life are important considerations. Additionally, it has been used as a stabilizer in fuels and lubricants to prevent degradation from exposure to oxygen and other reactive substances.

Upstream product

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• 1020-31-1 3,5-Di-tert-butylcatechol 
• 873055-54-0 carbonic acid 2,4-di-tert-butyl-phenyl ester methyl ester 
• 20039-94-5 2,4-di-tert-butyl-6-nitrophenol 
• 201023-39-4 cyclo-L-phenylalanyl-L-phenylalanine 
• 52184-29-9 2-nitro-4-chloro-2'-hydroxy-3',5'-di-tert-butylazobenzene 
• 52184-14-2 2,4-bis(1,1-dimethylethyl)-6-[(2-nitrophenyl)diazenyl]phenol 
• 325463-16-9 3,5-di-tert-butyl-1,2-benzoquinone 1-oxime 
• 52749-93-6 4-azido-2,4,6-tri-t-butyl-2,5-cyclohexadien-1-one 
• 96-76-4 2,4-di-tert-Butylphenol 

Downstream Products

• 103661-06-9 2,4-di-tert-butyl-6-{[(2-hydroxyphenyl)methylene]amino}phenol 
• 132056-61-2 2,4-di-tert-butyl-6-<(5-chloro-2-hydroxy-α-methylbenzylidene)amino>phenol 
• 124980-83-2 4-(2-Hydroxy-3,5-di-tert-butylphenylimino)-2,6-di-tert-butyl-2,5-cyclohexadien-1-one 
• 86759-35-5 4,6-di-tert-butyl-N-(2-hydroxy-3,5-di-tert-butyl-phenyl)-o-iminobenzoquinone 
• 77358-25-9 5,7-Di-tert-butyl-2,3-dihydro-2-(<13C>methyl)-2,2-diphenyl-1,3,2λ⁵-benzoxazaphosphol 
• 86314-36-5 5,7-Di-tert-butyl-2-phenylspiro<1,3,2λ⁵-benzoxaphosphol-2(3H),5'-λ⁵-dibenzophosphol> 
• 36931-29-0 1,2-bis(3,5-di-tert-butyl-2-hydroxyphenyl)oxamide 

Relevant articles and documents

Molecular structures, DFT studies and their photophysical properties in solution and solid state. Microwave-assisted multicomponent synthesis of organotin bearing Schiff bases

A couple of luminescent organotin compounds derivated from ligands-ONO were obtained by multicomponent microwave assisted synthesis in short time (15 min) and good yields: ((E)-8, 8-8-diphenylbenzo[d] naphtho [1,2-h][1,3,6,2] dioxazastannonine (1) and (E)

Fluorescent Molecular Rotors of Organoboron Compounds from Schiff Bases: Synthesis, Viscosity, Reversible Thermochromism, Cytotoxicity, and Bioimaging Cells

We report the design, synthesis, and characterization of two new fluorescent molecular rotors of boron derived from Schiff bases: (2,4,8,10-tetra-tert-butyl-6-phenyldibenzo[d,h][1,3,6,2]dioxazaboronine (3) and 1,4-bis(2,4,8,10-tetra-tert-butyldibenzo[d,h][1,3,6,2]dioxazaboronin-6-yl)benzene (4), as well as the free ligand 2-[[(3,5-di-tert-butyl-2-hydroxyphenyl)imino]methyl]-4,6-di-tert-butylphenol 1. All compounds were fully characterized by NMR (1H,11B, and13C), IR, UV/vis, fluorescence spectroscopy, and high-resolution mass spectrometry. The crystal structures of 3 and 4 showed tetracoordinated boron atoms with semiplanar skeleton ligands. The free rotation of the fluorescent molecular rotor, only observed in the binuclear compound, was decreased with increasing viscosity, while the quantum yield was increased. Interestingly, the property of reversible thermochromism was found in organoboron 4 in the solid state. DFT calculations to determine the both complexes have free rotation around the CPh-B1 bond. The boron compounds 3 and 4 have shown low cytotoxicity activity in cell line A-431 and low green staining in cells.

Tridentate [ONO] tungsten coordination compound and optical application thereof

The invention provides a tridentate [ONO] tungsten coordination compound and optical application thereof, and the tridentate [ONO] tungsten coordination compound is divided into but not limited to three structures, namely a structure I, a structure II and

A new bis-phenolate mesoionic carbene ligand for early transition metal chemistry

We report the synthesis of a new pincer-type triazolylidene ligand precursor H3L[Cl] with redox-active 3,5-di-tert-butylphenolate substituents on a multigram scale following a converging ten-step route. The potential of this new mesoionic carbe