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Tetrachlorophthalic acid

Product Name
Tetrachlorophthalic acid
CAS No.
632-58-6
Chemical Name
Tetrachlorophthalic acid
Synonyms
TIMTEC-BB SBB001247;RARECHEM AL BO 1285;tetrachloro-phthalicaci;TETRACHLOROPHTHALIC ACID;Tetrachlorophthalicacid,hemih;TETRACHLOROPHTHALIC ACID HEMIHYDRATE;Tetrachlorophthalic Acid Hemihydrate>Tetrachloro-1,2-benzenedicarboxylic acid;3,4,5,6-tetrachloro-2-benzenedicarboxylicacid;3,4,5,6-tetrachloro-1,2-benzenedicarboxylicacid
CBNumber
CB4196965
Molecular Formula
C8H2Cl4O4
Formula Weight
303.91
MOL File
632-58-6.mol
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Tetrachlorophthalic acid Property

Melting point:
98°C
Boiling point:
418.21°C (rough estimate)
Density 
1.8331 (rough estimate)
refractive index 
1.5282 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
pka
0.55±0.32(Predicted)
color 
White
Water Solubility 
Sparingly soluble
Stability:
Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference
632-58-6(CAS DataBase Reference)
EPA Substance Registry System
Tetrachlorophthalic acid (632-58-6)
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Safety

Risk Statements 
36/37/38
Safety Statements 
36/37/39
RTECS 
TI2795000
HS Code 
2917.39.7000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TCI Chemical
Product number
T0070
Product name
Tetrachlorophthalic Acid Hemihydrate
Purity
>98.0%(T)
Packaging
25g
Price
$19
Updated
2024/03/01
TCI Chemical
Product number
T0070
Product name
Tetrachlorophthalic Acid Hemihydrate
Purity
>98.0%(T)
Packaging
500g
Price
$179
Updated
2024/03/01
TRC
Product number
T889700
Product name
3,4,5,6-TetrachlorophthalicAcid
Packaging
50g
Price
$75
Updated
2021/12/16
SynQuest Laboratories
Product number
2621-5-01
Product name
Tetrachlorophthalic acid
Packaging
25g
Price
$20
Updated
2021/12/16
SynQuest Laboratories
Product number
2621-5-01
Product name
Tetrachlorophthalic acid
Packaging
100g
Price
$50
Updated
2021/12/16
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Tetrachlorophthalic acid Chemical Properties,Usage,Production

Chemical Properties

colourless crystals

Uses

Dyes, intermediates.

General Description

Colorless plates.

Air & Water Reactions

Sparingly water soluble.

Reactivity Profile

A chlorinated organic 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 Tetrachlorophthalic 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 Tetrachlorophthalic acid are not available; Tetrachlorophthalic acid is probably combustible.

Tetrachlorophthalic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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Tetrachlorophthalic acid Suppliers

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View Lastest Price from Tetrachlorophthalic acid manufacturers

Career Henan Chemical Co
Product
Tetrachlorophthalic acid 632-58-6
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100KG
Release date
2020-01-08

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