CasNo.50-79-3,factory lower price 50-79-3,(50-79-3) Suppliers

100 Kilogram	Negotiable

Min.Order :100 Kilogram
Purity: 99%
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Keywords

2,5-Dichlorobenzoic acid 50-79-3 C7H4Cl2O2

Quick Details

Appearance:powder
Application: 50-79-3
PackAge:Depended
ProductionCapacity:300|Kilogram|Month
Storage:Refrigerator
Transportation:by air or by sea

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2,5-Dichlorobenzoic acid Basic information

Product Name:	2,5-Dichlorobenzoic acid
Synonyms:	2,5-DICHLOROBENZOIC ACID;RARECHEM AL BO 0355;2,5-dichloro-benzoicaci;1,2-DICHLOROBENZENE PESTANAL;2,5-Dichlorobenzoic acid, 98+%;Benzoic acid, 2,5-dichloro-;2,5-Dichlorobenzoic acid ,99%;2,5-Dichlorobenzoic acid,97%
CAS:	50-79-3
MF:	C7H4Cl2O2
MW:	191.01
EINECS:	200-065-7
Product Categories:	Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Phenylacetic acid;Organic acids;Acids & Esters;Chlorine Compounds;DAlphabetic;Alpha sort;D;DIA - DIC;Pesticides&Metabolites;C7;Carbonyl Compounds;Carboxylic Acids;intermediate
Mol File:	50-79-3.mol

2,5-Dichlorobenzoic acid Chemical Properties

mp	151-154 °C(lit.)
bp	301 °C(lit.)
Fp	300-302°C
Water Solubility	<0.1 g/100 mL at 19 ºC
BRN	973353
Stability:	Stable.
CAS DataBase Reference	50-79-3(CAS DataBase Reference)
NIST Chemistry Reference	Benzoic acid, 2,5-dichloro-(50-79-3)
EPA Substance Registry System	Benzoic acid, 2,5-dichloro-(50-79-3)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36-24/25
WGK Germany	3
RTECS	DG6825000
HS Code	29163900

MSDS Information

Provider	Language
2,5-Dichlorobenzoic acid	English
SigmaAldrich	English
ACROS	English
ALFA	English

2,5-Dichlorobenzoic acid Usage And Synthesis

Chemical Properties	white crystalline powder
General Description	Needles (from water) or white powder.
Air & Water Reactions	Insoluble in water.
Reactivity Profile	Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in 2,5-Dichlorobenzoic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.
Fire Hazard	Flash point data for 2,5-Dichlorobenzoic acid are not available; however, 2,5-Dichlorobenzoic acid is probably combustible.

2,5-Dichlorobenzoic acid Preparation Products And Raw materials

Preparation Products	Irsogladine
Raw materials	Potassium permanganate-->Paraformaldehyde-->1,2,4-Trichlorobenzene-->p-Dichlorobenzene-->2,5-DICHLOROBENZOYL CHLORIDE-->2,5-Dichlorobenzonitrile

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