2,3,6-TRICHLOROBENZOIC ACID

2,3,6-TRICHLOROBENZOIC ACID Basic information
Product Name:2,3,6-TRICHLOROBENZOIC ACID
Synonyms:2,3,6-Tba(the herbicide);2,3,6-TCB;2,3,6-TCBA;2,3,6-Trichlorbenzoesaeure;2,3,6-trichloro-benzoicaci;Acide trichlorobenzoique;acidetrichlorobenzoique;Benzabar
CAS:50-31-7
MF:C7H3Cl3O2
MW:225.46
EINECS:200-026-4
Product Categories:Aromatic acidAlphabetic;Herbicides;Pesticides&Metabolites;TP - TZ;MOF
Mol File:50-31-7.mol
2,3,6-TRICHLOROBENZOIC ACID Structure
2,3,6-TRICHLOROBENZOIC ACID Chemical Properties
Melting point 126-127 °C(lit.)
Boiling point 324.5±37.0 °C(Predicted)
density 1.5599 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility soluble in Methanol
pka1.25±0.25(Predicted)
form neat
color White to Light yellow to Light orange
Water Solubility 7.70g/L(20 ºC)
Stability:Stable under recommended storage conditions., Stable Under Recommended Storage C
CAS DataBase Reference50-31-7(CAS DataBase Reference)
EPA Substance Registry System2,3,6-Trichlorobenzoic acid (50-31-7)
Safety Information
Hazard Codes Xn,N
Risk Statements 22-51/53
Safety Statements 61
RIDADR UN 2811 6.1/PG 1
WGK Germany 2
RTECS DH7700000
HS Code 2916.39.7900
Hazardous Substances Data50-31-7(Hazardous Substances Data)
ToxicityAcute oral LD50 for rats 1,500 mg/kg (Hartley and Kidd, 1987), 650 mg/kg (RTECS, 1985).
MSDS Information
2,3,6-TRICHLOROBENZOIC ACID Usage And Synthesis
Chemical PropertiesA solid.
UsesAn all-purpose, non-selective, pre-emergent and early post-emergent herbicide.
UsesSystemic growth-regulator herbicide used for postemergence control of broad-leaved perennial and annual weeds in cereals and grass seed crops.
DefinitionA substituted benzoic acid that is a potent synthetic auxin.
HazardPoison; moderately toxic.
Safety ProfilePoison by intraperitoneal route.Moderately toxic by ingestion and subcutaneous routes.When heated to decomposition it emits toxic fumes ofClí. Used as an herbicide.
Environmental FatePhotolytic. Plimmer (1970) postulated that the irradiation of 2,3,6-trichlorobenzoic acid in methanol will undergo dechlorination forming 2,3-, 2,6- and 3,6-dichlorobenzoic acids. Further irradiation may yield 2- and 3-chlorobenzoic acids which may ultimately form benzoic acid (Plimmer, 1970).
Chemical/Physical. Reacts with alkalies and amines forming water-soluble salts.
2,3,6-TRICHLOROBENZOIC ACID Preparation Products And Raw materials
AURORA 4691 Dacthal ethyl 2,3,5,6-tetrachlorobenzoate AURORA 4759 RARECHEM AL BI 0208 CHLORTHAL MONOMETHYL ESTER SODIUM 2,3,6-TRICHLOROBENZOIC ACID,2,3,6-Trichlorobenzoic acid sodium,2,3,6-Trichlorobenzoic acid sodium salt AURORA 5523 DIMETHYL TETRACHLOROTEREPHTHALATE (RING-UL-14C) Chlorthal DIMETHYL-D6 TETRACHLOROTEREPHTHALATE AURORA 4763 2,3,6-TRICHLOROBENZOIC ACID DIMETHYLAMINE SALT 2,3,6-TRICHLOROBENZOIC ACID RARECHEM AL BO 0468 PENTACHLOROBENZOIC ACID RARECHEM AL BF 0208 AURORA 5547

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