Tecnazene

Basic Info

Common NameTecnazene(F05923)
2D Structure
FRCD IDF05923
CAS Number117-18-0
PubChem CID8330
FormulaC6HCl4NO2
IUPAC Name

1,2,4,5-tetrachloro-3-nitrobenzene

InChI Key

XQTLDIFVVHJORV-UHFFFAOYSA-N

InChI

InChI=1S/C6HCl4NO2/c7-2-1-3(8)5(10)6(4(2)9)11(12)13/h1H

Canonical SMILES

C1=C(C(=C(C(=C1Cl)Cl)[N+](=O)[O-])Cl)Cl

Isomeric SMILES

C1=C(C(=C(C(=C1Cl)Cl)[N+](=O)[O-])Cl)Cl

Synonyms
        
            TECNAZENE
        
            Tecnazen
        
            2,3,5,6-Tetrachloronitrobenzene
        
            Arena
        
            1,2,4,5-Tetrachloro-3-nitrobenzene
        
            117-18-0
        
            Folosan
        
            Fusarex
        
            Myfusan
        
            Hickstor
Classifies
                

                  
                    Pesticide
Update DateNov 13, 2018 17:07

Chemical Taxonomy

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassNitrobenzenes
Intermediate Tree NodesNot available
Direct ParentNitrobenzenes
Alternative Parents
Molecular FrameworkAromatic homomonocyclic compounds
SubstituentsNitrobenzene - Nitroaromatic compound - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - C-nitro compound - Organic nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic nitrogen compound - Organochloride - Organohalogen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group.

Properties

Property NameProperty Value
Molecular Weight260.879
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Complexity195
Monoisotopic Mass258.876
Exact Mass260.873
XLogP3.9
Formal Charge0
Heavy Atom Count13
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

MRLs

FoodProduct CodeCountryMRLsApplication DateNotes
WalnutJapan0.05ppm
PecanJapan0.05ppm
AlmondJapan0.05ppm
Japanese Radish,Roots(Including Radish)Japan0.05ppm
Other Citrus FruitsJapan0.05ppm
Milk & Dairy ProduceBritain0.05mg/kg
RadishesBritain0.05mg/kg
Jerusalem ArtichokesBritain0.05mg/kg
Other Terrestrial Mammals,Edible OffalJapan0.05ppm
Other Cucurbitaceous VegetablesJapan0.05ppm
Other Composite VegetablesJapan0.05ppm
Japanese Radish,Leaves(Including Radish)Japan0.05ppm
Meat, Fat & Preparations Of MeatBritain0.05mg/kg
Other Cereals Do Not Include RiceBritain0.05mg/kg
RiceBritain0.05mg/kg
MilletBritain0.05mg/kg
BuckwheatBritain0.05mg/kg
MaizeBritain0.05mg/kg
TriticaleBritain0.05mg/kg
OatsBritain0.05mg/kg

References

TitleJournalDatePubmed ID
Multiresidue pesticide analysis of botanical dietary supplements using salt-outacetonitrile extraction, solid-phase extraction cleanup column, and gaschromatography-triple quadrupole mass spectrometry.Anal Chem2013 May 723534560
Assessment of the stability of pesticides during the cryogenic processing offruits and vegetables.Food Addit Contam2007 Nov17852403
Ion chromatographic determination of the decomposition products of tecnazenesolution irradiated by ultraviolet light: inorganic and organic anions.J Agric Food Chem2001 Jun11409977
The carry-through of residues of thiabendazole, tecnazene and chlorpropham frompotatoes following manufacture into potato crisps and jacket potato crisps.Food Addit Contam1996 Feb-Mar9064247
Determination of pesticide residues in food with a 6% cyanopropylphenyl capillarycolumn.J Chromatogr Sci1989 Feb2925828