ChemicalBook >> CAS DataBase List >>2,6-Dichlorobenzoic acid

2,6-Dichlorobenzoic acid

CAS No.
50-30-6
Chemical Name:
2,6-Dichlorobenzoic acid
Synonyms
AI3-33337;NSC 76599;CCRIS 8610;BRN 0973858;2,6-Dichlorobe;2,6-dichlorobenzoic;RARECHEM AL BO 0023;TIMTEC-BB SBB007694;2,6-dichlorobenzoate;2,6-Dichlorbenzoesure
CBNumber:
CB1673902
Molecular Formula:
C7H4Cl2O2
Molecular Weight:
191.01
MDL Number:
MFCD00002418
MOL File:
50-30-6.mol
Last updated:2024-04-22 13:56:47

2,6-Dichlorobenzoic acid Properties

Melting point 139-142 °C (lit.)
Boiling point 273.68°C (rough estimate)
Density 1.4410 (rough estimate)
refractive index 1.4590 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility 14g/l
form Fine Crystalline Powder
pka 1.69±0.10(Predicted)
color White to beige
Water Solubility 0.1-1 g/100 mL at 19 ºC
BRN 973858
Stability Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference 50-30-6(CAS DataBase Reference)
FDA UNII 634RI764QT
NIST Chemistry Reference Benzoic acid, 2,6-dichloro-(50-30-6)
EPA Substance Registry System Benzoic acid, 2,6-dichloro- (50-30-6)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-24/25-37/39
WGK Germany  3
RTECS  DG7000000
HazardClass  IRRITANT
HS Code  29163900
NFPA 704
0
2 0

2,6-Dichlorobenzoic acid price More Price(38)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich D57450 2,6-Dichlorobenzoic acid 98% 50-30-6 25g $18.72 2024-03-01 Buy
TCI Chemical D0339 2,6-Dichlorobenzoic Acid >98.0%(GC)(T) 50-30-6 5g $16 2024-03-01 Buy
TCI Chemical D0339 2,6-Dichlorobenzoic Acid >98.0%(GC)(T) 50-30-6 25g $40 2024-03-01 Buy
Alfa Aesar A10542 2,6-Dichlorobenzoic acid, 98% 50-30-6 25g $48.65 2024-03-01 Buy
Alfa Aesar A10542 2,6-Dichlorobenzoic acid, 98% 50-30-6 5g $17.4 2021-12-16 Buy
Product number Packaging Price Buy
D57450 25g $18.72 Buy
D0339 5g $16 Buy
D0339 25g $40 Buy
A10542 25g $48.65 Buy
A10542 5g $17.4 Buy

2,6-Dichlorobenzoic acid Chemical Properties,Uses,Production

Chemical Properties

white to off-white crystalline powder

Uses

2,6-Dichlorobenzoic Acid is an di-halogenated benzoic acid derivative and is used in the synthesis of Lux-S enzyme inhibitor.

Definition

ChEBI: 2,6-dichlorobenzoic acid is a chlorobenzoic acid carrying two chloro groups at positions 2 and 6 respectively. It has a role as a bacterial xenobiotic metabolite. It is a chlorobenzoic acid and a dichlorobenzene. It is functionally related to a benzoic acid. It is a conjugate acid of a 2,6-dichlorobenzoate.

Preparation

2,6-Dichlorobenzoic Acid can be prepared through several synthetic routes. One common method is the chlorination of benzoic acid in the presence of a catalyst such as phosphorus pentachloride or thionyl chloride. The reaction takes place under reflux in anhydrous conditions, resulting in the substitution of two chlorine atoms at positions 2 and 6 of the benzene ring. The resulting product is then isolated and purified through recrystallization from a suitable solvent. Another method involves the chlorination of the methyl ester of 2,6-dichlorobenzoic acid, followed by hydrolysis to yield the desired compound. Alternatively, it can also be synthesized through the oxidation of 2,6-dichlorotoluene using potassium permanganate or other oxidizing agents.

Air & Water Reactions

Slightly soluble in water.

Reactivity Profile

2,6-Dichlorobenzoic acid is a halogenated carboxylic acid. 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 2,6-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 2,6-Dichlorobenzoic acid are not available; however, 2,6-Dichlorobenzoic acid is probably combustible.

Purification Methods

Crystallise the acid from EtOH and sublime it in vacuo.[Beilstein 9 IV 1005.] Aromatic acid impurities (to <0.05%) can be removed via the (±)--methylbenzylamine salt as described for 2,4-dichlorobenzoic acid [Ley & Yates Organic Process Research & Development 12 120 2008.]

Global( 393)Suppliers
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Henan Allgreen Chemical Co.,LTD
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Hefei TNJ Chemical Industry Co.,Ltd.
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View Lastest Price from 2,6-Dichlorobenzoic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,6-Dichlorobenzoic acid pictures 2024-04-26 2,6-Dichlorobenzoic acid
50-30-6
US $35.00 / KG 1KG 98% 20 tons Speranza Chemical Co., Ltd.
2,6-Dichlorobenzoic acid pictures 2024-04-22 2,6-Dichlorobenzoic acid
50-30-6
US $30.00 / kg 1kg 99.7% 200000kg Ouhuang Engineering Materials (Hubei) Co., Ltd
4-Benzoylbiphenyl pictures 2024-04-22 4-Benzoylbiphenyl
50-30-6
US $30.00 / kg 1kg 99.7% 200000kg Ouhuang Engineering Materials (Hubei) Co., Ltd
  • 4-Benzoylbiphenyl pictures
  • 4-Benzoylbiphenyl
    50-30-6
  • US $30.00 / kg
  • 99.7%
  • Ouhuang Engineering Materials (Hubei) Co., Ltd
2,6-DICHLOROBENZOIC ACID TIMTEC-BB SBB007694 RARECHEM AL BO 0023 2,6-dichlorobenzoic 2,6-dichloro-benzoicaci Benzoicacid,2,6-dichloro- TEPP PESTANAL (TETRAETHYL PYRO- PHOSPHAT 2,6-Dichlorobenzoicacid,98% 2,6-Dichlorobenzoic acid, 98+% 25GR 2,6-DICLOROBENZOIC ACID 2,6-Dichlorobenzoic Acid, 97+% 2,6-Dichlorobe 2,6-dichlorobenzoate AI3-33337 BRN 0973858 CCRIS 8610 NSC 76599 2,6-Dichlorobenzoic acid Benzoic acid, 2,6-dichloro- AI3-33337 BRN 0973858 CCRIS 8610 NSC 76599 2,6-dichlorobenzoate 2,6-Dichlorobenzoic Acid > 2,6-Dichlorbenzoesure Lincomycin Impurity 1 Hydrochloride(Lincomycin EP Impurity D Hydrochloride) 50-30-6 50-30-0 C7H4O2Cl2 Organic Building Blocks Building Blocks Carbonyl Compounds Carboxylic Acids C7 C7 Carbonyl Compounds Carboxylic Acids Alpha sort D DAlphabetic DIA - DIC Pesticides&Metabolites intermediate FINE Chemical & INTERMEDIATES