121-91-5 C8H6O4 ...

121-91-5    C8H6O4    Isophthalic acid
121-91-5    C8H6O4    Isophthalic acid
121-91-5    C8H6O4    Isophthalic acid
121-91-5    C8H6O4    Isophthalic acid
121-91-5    C8H6O4    Isophthalic acid

121-91-5 C8H6O4 Isophthalic acid

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10 Gram

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  • Min.Order :10 Gram
  • Purity: 99%
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Keywords

121-91-5 C8H6O4 Isophthalic acid 121-91-5 C8H6O4

Quick Details

  • Appearance:white powder
  • Application:Building Blocks;C8;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks
  • PackAge:Woven bag
  • ProductionCapacity:1|Kilogram|Day
  • Storage:Normal temperature
  • Transportation:Ocean shipping Express delivery

Superiority:

 
Isophthalic acid Basic information
Product Name: Isophthalic acid
Synonyms: RARECHEM AL BO 0036;M-PHTHALIC ACID;1,3-dicarboxybenzene;1,3-phthalicacid;Acide isophtalique;acideisophtalique;acideisophtalique(french);isophthalate
CAS: 121-91-5
MF: C8H6O4
MW: 166.13
EINECS: 204-506-4
Product Categories: Building Blocks;C8;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks
Mol File: 121-91-5.mol
Isophthalic acid Structure
 
Isophthalic acid Chemical Properties
mp  341-343 °C(lit.)
density  1,54 g/cm3
Water Solubility  0.01 g/100 mL (25 ºC)
Merck  14,5197
BRN  1909332
Stability: Stable. Incompatible with strong oxidizing agents, strong bases.
CAS DataBase Reference 121-91-5(CAS DataBase Reference)
NIST Chemistry Reference 1,3-Benzenedicarboxylic acid(121-91-5)
EPA Substance Registry System 1,3-Benzenedicarboxylic acid(121-91-5)
 
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  24/25-36-26
WGK Germany  2
RTECS  NT2007000
HS Code  29173980
Hazardous Substances Data 121-91-5(Hazardous Substances Data)
MSDS Information
Provider Language
1,3-Benzenedicarboxylic acid English
ACROS English
SigmaAldrich English
ALFA English
 
Isophthalic acid Usage And Synthesis
Chemical Properties whitetolightyellowcrytalpowe
Usage Purified Isophthalic Acid (PIA) is mainly used as intermediate for high performance UPR, resins for coatings, high solids paints, gel coats, modifier of PET for bottles. Product Data Sheet
General Description White solid with a slight unpleasant odor. Sinks in water.
Air & Water Reactions Dust forms explosive mixture in air [USCG, 1999].
Reactivity Profile Isophthalic acid is a 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 Isophthalic 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.
Health Hazard May cause slight to moderate irritation of eyes, skin, and mucous membranes on prolonged contact. Ingestion may cause gastrointestinal irritation.
Fire Hazard Behavior in Fire: Dust forms explosive mixture in air.

 

Details:

 
Isophthalic acid Basic information
Product Name: Isophthalic acid
Synonyms: RARECHEM AL BO 0036;M-PHTHALIC ACID;1,3-dicarboxybenzene;1,3-phthalicacid;Acide isophtalique;acideisophtalique;acideisophtalique(french);isophthalate
CAS: 121-91-5
MF: C8H6O4
MW: 166.13
EINECS: 204-506-4
Product Categories: Building Blocks;C8;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks
Mol File: 121-91-5.mol
Isophthalic acid Structure
 
Isophthalic acid Chemical Properties
mp  341-343 °C(lit.)
density  1,54 g/cm3
Water Solubility  0.01 g/100 mL (25 ºC)
Merck  14,5197
BRN  1909332
Stability: Stable. Incompatible with strong oxidizing agents, strong bases.
CAS DataBase Reference 121-91-5(CAS DataBase Reference)
NIST Chemistry Reference 1,3-Benzenedicarboxylic acid(121-91-5)
EPA Substance Registry System 1,3-Benzenedicarboxylic acid(121-91-5)
 
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  24/25-36-26
WGK Germany  2
RTECS  NT2007000
HS Code  29173980
Hazardous Substances Data 121-91-5(Hazardous Substances Data)
MSDS Information
Provider Language
1,3-Benzenedicarboxylic acid English
ACROS English
SigmaAldrich English
ALFA English
 
Isophthalic acid Usage And Synthesis
Chemical Properties whitetolightyellowcrytalpowe
Usage Purified Isophthalic Acid (PIA) is mainly used as intermediate for high performance UPR, resins for coatings, high solids paints, gel coats, modifier of PET for bottles. Product Data Sheet
General Description White solid with a slight unpleasant odor. Sinks in water.
Air & Water Reactions Dust forms explosive mixture in air [USCG, 1999].
Reactivity Profile Isophthalic acid is a 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 Isophthalic 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.
Health Hazard May cause slight to moderate irritation of eyes, skin, and mucous membranes on prolonged contact. Ingestion may cause gastrointestinal irritation.
Fire Hazard Behavior in Fire: Dust forms explosive mixture in air.
   HenNan sunlake enterprise corporation is located in Henan Province , The central plain of China , Which enjoys favorable geogeaphical position and convenient transportion, The com[any was established in june. 1998 , until now having more than 18 years experience in manufacturing & exporting chemical raw material . 
   Sunlake is a professional manufacturer engaged in producing and selling chemicals,including Organic & inorganic chemicals , pigments & Dyestuffs , Water treatment chemicals , Food & FEED additives and others . these products have been being well exported to europe , southeast Asia , the Middle East , Africa , South America and some other countries and areas. 
    We sincerely welcome foreign friends to visit our plant for cooperation. With the idea of "quality first,credit priority, Excellent service", We are highly acknowledged by customers for good quality and competitive price. More importantly , the company has a strong R & D team, who are professional engineers and scholars with Ph. D. .So we are confident to serve you better with our high - quality products and professional team. 
     We are taking great efforts to provide our customers with demanded goods and professional services, and continuously improve our core ability of competition and get the momentum for sustainable development, and finally make us being a reliable and professional wupplier in international market. 
We welcome any serious inquiries from all customers of the world, and sincerely hope to cooperate with you for a brilliant future!
 

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