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Bis(2,4,6-trichlorophenyl) oxalate - for chemiluminescence, ≥99.0% (AT), high purity , CAS No.1165-91-9

In stock
Item Number
B121486
Grouped product items
SKU Size
Availability
Price Qty
B121486-1g
1g
3
$103.90
B121486-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$274.90
B121486-25g
25g
3
$892.90
B121486-100g
100g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$2,197.90
View related series
Spectroscopic reagent (233)

Basic Description

Synonyms TCPO | DTXSID80151403 | FT-0622986 | Bis(2,4,6-trichlorophenyl) oxalate | 2,4,6-Trichlorophenyl oxalate | Ethanedioic acid, bis(2,4,6-trichlorophenyl) ester | Ethanedioic acid, 1,2-bis(2,4,6-trichlorophenyl) ester | Bis(2,4,6-trichlorophenyl) ethanedioate
Specifications & Purity for chemiluminescence, ≥99%(AT)
Storage Temp Protected from light,Argon charged
Shipped In Normal
Grade for chemiluminescence
Product Description

Chemiluminescence: Emission: 430 nm (reaction of TCPO with 9,10-Diphenylanthracene and H2O2)
Chemiluminescence reagent for the determination of fluorescent compounds

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Phenoxyacetic acid derivatives
Intermediate Tree Nodes Not available
Direct Parent Phenoxyacetic acid derivatives
Alternative Parents Phenol esters  Phenoxy compounds  Chlorobenzenes  Dicarboxylic acids and derivatives  Aryl chlorides  Carboxylic acid esters  Organochlorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Phenoxyacetate - Phenol ester - Phenoxy compound - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Dicarboxylic acid or derivatives - Carboxylic acid ester - Carboxylic acid derivative - Organochloride - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Organohalogen compound - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as phenoxyacetic acid derivatives. These are compounds containing an anisole where the methane group is linked to an acetic acid or a derivative.
External Descriptors Not available

Names and Identifiers

Pubchem Sid 504757486
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504757486
IUPAC Name bis(2,4,6-trichlorophenyl) oxalate
INCHI InChI=1S/C14H4Cl6O4/c15-5-1-7(17)11(8(18)2-5)23-13(21)14(22)24-12-9(19)3-6(16)4-10(12)20/h1-4H
InChIKey GEVPIWPYWJZSPR-UHFFFAOYSA-N
Smiles C1=C(C=C(C(=C1Cl)OC(=O)C(=O)OC2=C(C=C(C=C2Cl)Cl)Cl)Cl)Cl
Isomeric SMILES C1=C(C=C(C(=C1Cl)OC(=O)C(=O)OC2=C(C=C(C=C2Cl)Cl)Cl)Cl)Cl
WGK Germany 3
Molecular Weight 448.9
Beilstein 2312135
Reaxy-Rn 2312135
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2312135&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot Number Certificate Type Date Item
K2219189 Certificate of Analysis Sep 16, 2022 B121486
I2418113 Certificate of Analysis Sep 16, 2022 B121486
K2219190 Certificate of Analysis Sep 16, 2022 B121486
K2221064 Certificate of Analysis Sep 16, 2022 B121486
K2219183 Certificate of Analysis Sep 16, 2022 B121486
J1825222 Certificate of Analysis Aug 12, 2022 B121486
B2211141 Certificate of Analysis Dec 10, 2021 B121486
B2211196 Certificate of Analysis Dec 10, 2021 B121486
B2211125 Certificate of Analysis Dec 10, 2021 B121486
B2211195 Certificate of Analysis Dec 10, 2021 B121486

Chemical and Physical Properties

Sensitivity Moisture and light sensitive
Melt Point(°C) 187-193°C
Molecular Weight 448.900 g/mol
XLogP3 7.300
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 5
Exact Mass 447.821 Da
Monoisotopic Mass 445.824 Da
Topological Polar Surface Area 52.600 Ų
Heavy Atom Count 24
Formal Charge 0
Complexity 412.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Yuyuan Zhang, Jing Lei, Wei Liu, Yan Jin, Baoxin Li.  (2022)  Chemiluminescence resonance energy transfer as a simple and sensitive readout mode for a CRISPR/Cas12a-based biosensing platform.  ANALYST,  147  (24): (5687-5693). 
2. Hongyan Tan, Hong Zhou, Donghua Chen.  (2022)  A peroxyoxalate chemiluminescence recovery system based on the interaction of N-doped graphene oxide nanosheets and an oligopeptide for ultra-sensitive and selective copper(II) ion detection.  Analytical Methods,  14  (19): (1897-1903). 
3. Yaxin Zhao, Yuyu Ma, Yinhuan Li.  (2022)  Chemiluminescence resonance energy transfer determination of uric acid with fluorescent covalent organic framework as energy acceptor.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,  268  (120643). 
4. Guihua Zhang, Xinyi Zou, Hua Li, Yi He.  (2021)  Visual colorimetric detection of triacetone triperoxide based on a Fe(II)-promoted thermal decomposition process.  ANALYST,  146  (20): (6187-6192). 
5. Lingfei Li, Dan Lin, Fan Yang, Youyu Xiao, Liang Yang, Shaoming Yu, Changlong Jiang.  (2021)  Gold Nanoparticle-Based Peroxyoxalate Chemiluminescence System for Highly Sensitive and Rapid Detection of Thiram Pesticides.  ACS Applied Nano Materials,  (4): (3932–3939). 
6. Chen Donghua, Wen Siming, Peng Rulin, Gong Qingsong, Fei Junjie, Fu Zhuo, Weng Chao, Liu Minna.  (2019)  A triple signal amplification method for chemiluminescent detection of the cancer marker microRNA-21.  MICROCHIMICA ACTA,  186  (7): (1-8). 
7. Chen Donghua, Peng Rulin, Zhou Hong, Liu Hui.  (2016)  Sensitive determination of 4-nitrophenol based on its enhancement of a peroxyoxalate chemiluminescence system containing graphene oxide quantum dots and fluorescein.  MICROCHIMICA ACTA,  183  (5): (1699-1704). 

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