4956-41-6

Basic information

• Product Name: 1 2-BIS(OCTYLOXY)BENZENE 97
• Synonyms: 1 2-BIS(OCTYLOXY)BENZENE 97
• CAS NO: 4956-41-6
• Molecular Formula: C₂₂H₃₈O₂
• Molecular Weight: 334.54
• Product Categories: Ethers;Organic Building Blocks;Oxygen Compounds;Building Blocks;C20 to C60+;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds
• Mol File: 4956-41-6.mol
• Article Data: 49

Chemical Properties

• Boiling Point: 332-333 °C(lit.)
• Flash Point: 187 °F
• Appearance: /
• Density: 0.904 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.000285mmHg at 25°C
• Refractive Index: n20/D 1.4840(lit.)
• CAS DataBase Reference: 1 2-BIS(OCTYLOXY)BENZENE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 1 2-BIS(OCTYLOXY)BENZENE 97(4956-41-6)
• EPA Substance Registry System: 1 2-BIS(OCTYLOXY)BENZENE 97(4956-41-6)

Safety Data

• RIDADR: NA 1993 / PGIII
• WGK Germany: 3
• Hazardous Substances Data: 4956-41-6(Hazardous Substances Data)

Usage

General Description

1 2-BIS(OCTYLOXY)BENZENE 97 is a chemical compound also known as bis(2-octyloxyphenyl) benzene, which is a clear, colorless liquid with a molecular weight of 398.64 g/mol. It is primarily used as a plasticizer and as a component in the production of various polymers and resins. The compound is insoluble in water but soluble in most organic solvents. It is also used in the manufacturing of adhesives, sealants, and coatings, and as a stabilizer in the production of PVC and other plastics. 1 2-BIS(OCTYLOXY)BENZENE 97 is known for its high thermal stability and is preferred in applications where heat resistance is crucial. It is important to handle this compound with care and adhere to proper safety protocols, as it may pose health hazards if not handled properly.

InChI:InChI=1/C22H38O2/c1-3-5-7-9-11-15-19-23-21-17-13-14-18-22(21)24-20-16-12-10-8-6-4-2/h13-14,17-18H,3-12,15-16,19-20H2,1-2H3

Upstream product

• 111-83-1 1-bromo-octane 
• 120-80-9 benzene-1,2-diol 
• 111-87-5 octanol 
• 3386-35-4 1-octyl p-toluenesulfonate 
• 34789-97-4 pyrocatechol monosodium salt 

Downstream Products

• 70351-86-9 2,3,6,7,10,11-hexakis(hexyloxy)triphenylene 
• 70351-87-0 2,3,6,7,10,11-hexakis(octyloxy)triphenylene 
• 4956-40-5 3,4-di(octyloxy)nitrobenzene 
• 118132-04-0 1,2-Dibromo-4,5-bis(octyloxy)benzene 
• 111195-33-6 3,4-di-n-octyloxyacetophenone 
• 111195-34-7 3,4-Bis-octyloxy-benzoic acid ethyl ester 
• 131525-56-9 3,4-bis(octyloxy)benzoic acid 
• 1185259-37-3 1-[3,4-bis(octyloxy)phenyl]-1-(4-nitrophenyl)methanone 
• 1185259-39-5 1-[4-(methylsulfonyl)phenyl]-1-[3,4-bis(octyloxy)phenyl]methanone 
• 1185259-36-2 4-[3,4-bis(octyloxy)benzoyl]benzonitrile 
• 1185259-38-4 (3-nitrophenyl)[3,4-bis(octyloxy)phenyl]methanone 
• 1161208-37-2 1-(3,4-bis-octyloxyphenyl)-5-bromopentan-1-one 
• 1161208-76-9 methyl 4-[3,4-bis(octyloxy)benzoyl]benzoate 
• 1185259-35-1 dimethyl 5-[3,4-bis(octyloxy)benzoyl]benzene-1,3-dioate 

Relevant articles and documents

Iridium-based emitters containing pendant triphenylene moieties for bluish-green OLEDs with improved efficiency upon thermal annealing

Two new cyclometalated iridium complexes with non-conjugated triphenylene moieties attached to the ancillary ligand, namely YF3 and YF4, are reported. Both iridium complexes presented intense bluish-green emission both in solution (ΦPL ～ 0.37-0

Investigation of Optical and Electrochemical Properties of Benzene Based Solution Processable 2,1,3-Benzooxadiazole Comprising Polymers

Four novel solution processable benzooxadiazole containing alternating copolymers namely poly (5,6-bis(octyloxy)-4-(5-phenylthiophen-2-yl)-7-(thiophen-2-yl)benzo[c][1,2,5]oxadiazole)PBOTPh, poly (5,6-bis(octyloxy)-4-(5-phenylselenophen-2-yl)-7-(selenophen

Constructing a self-assembling C3-symmetric covalently linked (fused) donor-acceptor-type molecule containing a hexaazatriphenylene core

A C3-symmetric covalently linked (fused) molecule, HAT-IPN, comprising a 13 fused ring system was synthesized by a condensation-cyclisation reaction between hexaazatriphenylenehexacarboxylic acid trisanhydride and 4,5-diamino-1,2-dioctyloxybenzene. This fused system exhibits ambipolar behaviour due to an n-type HAT-core at the center and three outer p-type fused dialkoxybenzimidazole moieties, which is confirmed by cyclic voltammetry. The self-assembling nature of this disc-shaped donor-acceptor type system is evident in13C NMR spectroscopy, dynamic light scattering studies, differential scanning calorimetry and atomic force microscopy (AFM) images, which illustrate the formation of the one-dimensional aggregates both in solution and in the film state; indicating its potential as an active component in organic electronic devices.