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Technology Process of Butyl octyl phthalate

Butyl octyl phthalate

Base Information
  • Chemical Name:Butyl octyl phthalate
  • CAS No.:84-78-6
  • Molecular Formula:C20H30O4
  • Molecular Weight:334.456
  • Hs Code.:2917349000
  • European Community (EC) Number:201-562-1
  • NSC Number:69894
  • UNII:Y52J9Q533Y
  • DSSTox Substance ID:DTXSID2052578
  • Nikkaji Number:J192.618G
  • Wikidata:Q27294278
  • Mol file:84-78-6.mol
Butyl octyl phthalate

Synonyms:Butyl octyl phthalate;84-78-6;Plasticizer OBP;Staflex BOP;Octyl butyl phthalate;Plasticizer BOP;Truflex OBP;1,2-Benzenedicarboxylic acid, butyl octyl ester;PX 914;Phthalic acid, butyl octyl ester;1-O-butyl 2-O-octyl benzene-1,2-dicarboxylate;NSC 69894;EINECS 201-562-1;BRN 2289337;1,2-Benzenedicarboxylic acid, 1-butyl 2-octyl ester;UNII-Y52J9Q533Y;Phthalic acid, butyloctyl ester;Butyl octyl phthalate(Technical);Y52J9Q533Y;NSC-69894;butyloctylphthalat-;1, butyl octyl ester;SCHEMBL50451;Cbz-DL-3-Aminoisobutyricacid;1-Butyl 2-octyl phthalate #;DTXSID2052578;AMY28401;NSC69894;MFCD00072261;Phthalic acid 1-butyl 2-octyl ester;AS-57441;LS-29757;1-butyl 2-octyl benzene-1,2-dicarboxylate;CS-0134595;C13887;A928579;Phthalic acid, butyl octyl ester (6CI,7CI,8CI);Q27294278

Suppliers and Price of Butyl octyl phthalate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Crysdot
  • Butyloctylphthalate 95+%
  • 100g
  • $ 49.00
  • American Custom Chemicals Corporation
  • BUTYL OCTYL PHTHALATE 95.00%
  • 5MG
  • $ 503.16
  • Ambeed
  • Butyloctylphthalate 95%
  • 1g
  • $ 171.00
  • Ambeed
  • Butyloctylphthalate 95%
  • 250mg
  • $ 72.00
Total 26 raw suppliers
Chemical Property of Butyl octyl phthalate
Chemical Property:
  • Vapor Pressure:6.93E-06mmHg at 25°C 
  • Boiling Point:377.1°C at 760 mmHg 
  • Flash Point:200.1°C 
  • PSA：52.60000 
  • Density:1.012g/cm3 
  • LogP:5.16080 
  • Storage Temp.:Sealed in dry,Room Temperature 
  • XLogP3:6.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:14
  • Exact Mass:334.21440943
  • Heavy Atom Count:24
  • Complexity:354
Purity/Quality:

99% *data from raw suppliers

Butyloctylphthalate 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC
Technology Process of Butyl octyl phthalate

There total 1 articles about Butyl octyl phthalate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

1,2-benzenedicarboxylic acid 1-butyl 2-octyl ester
84-78-6

1,2-benzenedicarboxylic acid 1-butyl 2-octyl ester

Guidance literature:
Phthalsaeure-monobutylester-triethylamin-Salz, Octylchlorid;
Refernces

Study of Anopheles gambiae 3-hydroxykynurenine transaminase activity and inhibition by LC-MS/MS method

10.1016/j.jpba.2019.05.025

The study focuses on the activity and inhibition of Anopheles gambiae 3-hydroxykynurenine transaminase (Ag-HKT), an enzyme that metabolizes 3-hydroxykynurenine into xanthurenic acid, which is crucial for mosquito vector physiology and a potential target for transmission-blocking drugs and insecticides. The researchers developed and validated a new LC-MS/MS method to evaluate Ag-HKT activity and the potency of inhibitors. Chemicals used in the study included L-kynurenine (L-KYN), kynurenic acid (KA), xanthurenic acid (XA), 3-hydroxy-DL-kynurenine (D,L-3-HK), and pyridoxal 5′-phosphate (PLP) as key components of the enzymatic assay. Additionally, 4-(2-aminophenyl)-4-oxobutanoic acid (INI) and its derivative 4-(2-Amino-3-hydroxyphenyl)-4-oxobutanoic acid (3-OH-INI) were synthesized and tested as potential inhibitors of Ag-HKT. The purpose of these chemicals was to establish a method for quantifying the enzyme's activity and to identify and characterize compounds that could inhibit Ag-HKT, providing a basis for the development of new insecticides and malaria transmission-blocking drugs.

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