ChemicalBook > CAS DataBase List > Isophthalic acid

Isophthalic acid

Product Name
Isophthalic acid
CAS No.
121-91-5
Chemical Name
Isophthalic acid
Synonyms
1,3-BENZENEDICARBOXYLIC ACID;Isophthalic;isophthalate;M-PHTHALIC ACID;1,3-phthalicacid;1,3-dicarboxybenzene;IPA)Isophthalic;sophthalic acid;ISOPHTHALIC ACID;META-PHTHALICACID
CBNumber
CB3262667
Molecular Formula
C8H6O4
Formula Weight
166.13
MOL File
121-91-5.mol
More
Less

Isophthalic acid Property

Melting point:
341-343 °C (lit.)
Boiling point:
214.32°C (rough estimate)
Density 
1,54 g/cm3
vapor pressure 
0Pa at 25℃
refractive index 
1.5100 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
0.12g/l
form 
Crystalline Powder
pka
3.54(at 25℃)
color 
White to off-white
PH
3.33(1 mM solution);2.76(10 mM solution);2.24(100 mM solution)
Water Solubility 
0.01 g/100 mL (25 ºC)
Merck 
14,5197
BRN 
1909332
Dielectric constant
1.4(Ambient)
Stability:
Stable. Incompatible with strong oxidizing agents, strong bases.
InChIKey
QQVIHTHCMHWDBS-UHFFFAOYSA-N
LogP
1.66 at 25℃
CAS DataBase Reference
121-91-5(CAS DataBase Reference)
NIST Chemistry Reference
1,3-Benzenedicarboxylic acid(121-91-5)
EPA Substance Registry System
Isophthalic acid (121-91-5)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
24/25-36-26
WGK Germany 
2
RTECS 
NT2007000
Autoignition Temperature
1198 °F
TSCA 
Yes
HS Code 
29173980
Hazardous Substances Data
121-91-5(Hazardous Substances Data)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

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

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

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
I19209
Product name
Isophthalic acid
Purity
99%
Packaging
2kg
Price
$98.9
Updated
2024/03/01
Sigma-Aldrich
Product number
42304
Product name
Isophthalic acid
Purity
analytical standard
Packaging
50mg
Price
$73.5
Updated
2022/05/15
TCI Chemical
Product number
I0155
Product name
Isophthalic Acid
Purity
>99.0%(GC)(T)
Packaging
25g
Price
$18
Updated
2024/03/01
TCI Chemical
Product number
I0155
Product name
Isophthalic Acid
Purity
>99.0%(GC)(T)
Packaging
500g
Price
$29
Updated
2024/03/01
Alfa Aesar
Product number
A14445
Product name
Isophthalic acid, 99%
Packaging
250g
Price
$23.3
Updated
2024/03/01
More
Less

Isophthalic acid Chemical Properties,Usage,Production

Description

Isophthalic acid is an organic compound with the formula C6H4(CO2H)2. This colourless solid is an isomer of phthalic acid and terephthalic acid. These aromatic dicarboxylic acids are used as precursors (in form of acyl chlorides) to commercially important polymers, e.g. the fire-resistant material Nomex. Mixed with terephthalic acid, iso phthalic acid is used in the production of resins for drink bottles. The high-performance polymer poly benzimidazole is produced from iso phthalic acid.

Chemical Properties

Isophthalic acid is a white crystalline powder or needle-like crystals and it’s an isomer of phthalic acid and terephthalic acid.It is insoluble in cold water but soluble in oxygenated solvents and alcohol. It is combustible and finely dispersed particles will form explosive mixtures in air.

Isophthalic Acid (PIA) is mainly used in the production of bottle PET, also used in the production of alkyd resin, polyester resin, also used in the production of photosensitive materials, pharmaceutical intermediates and so on.
One of the largest applications for PIA is in unsaturated polyester resins for high-quality gel coats. The hardness, stain and detergent resistance characteristics of PIA are ideal for polyester solid-surface countertops that are an inexpensive alternative to acrylics.

Uses

Isophthalic acid is used as an intermediate for high performance unsaturated polyesters, resins for coatings, high solids paints, gel coats and modifier of polyethylene terephthalate for bottles. It acts as precursors for the fire-resistant material nomex as well as used in the preparation of high-performance polymer polybenzimidazole. It is also employed as an input for the production of insulation materials.

Uses

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

Definition

ChEBI: A benzenedicarboxylic acid that is benzene substituted by carboxy groups at position 1 and 3. One of three possible isomers of benzenedicarboxylic acid, the others being phthalic and terephthalic acids.

Preparation

Iso phthalic acid is produced on the billion kilogram per year scale by oxidizing meta-xylene using oxygen . The process employs a cobalt-manganese catalyst. In the laboratory, chromic acid can be used as the oxidant. It also arises by fusing potassium meta-sulpho benzoate , or meta - brom benzoate with potassium formate (terephthalic acid is also formed in the last case).
The barium salt (as its hexa hydrate) is very soluble (a distinction between phthalic and terephthalic acids). Uvitic acid, 5- methylisophthalic acid, is obtained by oxidizing mesitylene or by condensing pyroracemic acid with baryta water.

Synthesis Reference(s)

Journal of the American Chemical Society, 82, p. 1911, 1960 DOI: 10.1021/ja01493a020

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.

Flammability and Explosibility

Non flammable

Purification Methods

Crystallise the acid from aqueous EtOH. [Beilstein 9 IV 3292.]

More
Less

Isophthalic acid Suppliers

TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32159
Advantage
58
Aladdin Scientific
Tel
Email
tp@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Sisco Research Laboratories Pvt. Ltd.
Tel
--
Fax
--
Email
srlmarketing@dishnetdsl.net
Country
United States
ProdList
1905
Advantage
64
Neuchem
Tel
--
Fax
--
Email
INFO@NEUCHEM.COM
Country
United States
ProdList
256
Advantage
58
Monomer Polymer & Dajac Labs
Tel
--
Fax
--
Email
info@monomerpolymer.com
Country
United States
ProdList
1609
Advantage
58
CJ Chemicals
Tel
--
Fax
--
Email
info@cjchemicals.net
Country
United States
ProdList
189
Advantage
58
Greenchem Industries LLC
Tel
--
Fax
--
Email
info@greenchemindustries.com
Country
United States
ProdList
61
Advantage
58
Command Chemical Corporation, Inc.
Tel
--
Fax
--
Email
info@commandchemical.com
Country
United States
ProdList
40
Advantage
58
Maroon Group (formerly D.B. Becker Co., Inc.)
Tel
--
Fax
--
Email
Info@maroongroupllc.com
Country
United States
ProdList
113
Advantage
58
SGA Specialties Group, L.L.C.
Tel
--
Fax
--
Email
sales@sgaspecialties.com
Country
United States
ProdList
26
Advantage
58
Redox Scientific
Tel
--
Fax
--
Email
info@redoxsci.com
Country
United States
ProdList
2380
Advantage
58
ICC Chemical Corporation (a subsidiary of ICC Industries Inc.)
Tel
--
Fax
--
Email
fkt@iccchem.com
Country
United States
ProdList
113
Advantage
58
Wego Chemical Group
Tel
--
Fax
--
Email
sales@wegochem.com
Country
United States
ProdList
443
Advantage
58
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
Brenntag North America, Inc.
Tel
--
Fax
--
Email
bnereadingcs@brenntag.com
Country
United States
ProdList
211
Advantage
58
Trinternational Inc
Tel
--
Fax
--
Email
info@trichemicals.com
Country
United States
ProdList
69
Advantage
58
Moravek, Inc.
Tel
--
Fax
--
Email
info@moravek.com
Country
United States
ProdList
279
Advantage
58
The Chemical Company (TCC)
Tel
--
Fax
--
Email
bsawicki@thechemco.com
Country
United States
ProdList
84
Advantage
58
Ivanhoe Industries Inc.
Tel
--
Fax
--
Email
info@ivanhoeindustries.com
Country
United States
ProdList
35
Advantage
58
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
Darwin Chemical Company
Tel
--
Fax
--
Email
shipping@darwinchemical.com
Country
United States
ProdList
69
Advantage
43
Sinova Inc.
Tel
--
Fax
--
Email
sales@sinovainc.com
Country
United States
ProdList
4009
Advantage
58
First Continental International (FCI)
Tel
--
Fax
--
Email
sales@fci-nj.com
Country
United States
ProdList
178
Advantage
58
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Chemceed Corportaion
Tel
--
Fax
--
Email
inquiry@chemceed.com
Country
United States
ProdList
175
Advantage
50
Chemstock Inc.
Tel
--
Fax
--
Email
mail@chemstock.com
Country
United States
ProdList
575
Advantage
34
Anvia Chemicals, LLC
Tel
--
Fax
--
Email
sales@anviachem.com
Country
United States
ProdList
3933
Advantage
0
Ivy Fine Chemicals
Tel
--
Fax
--
Email
sales@ivychem.com
Country
United States
ProdList
6493
Advantage
58
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60
ChemService Inc.
Tel
--
Fax
--
Country
United States
ProdList
6379
Advantage
68
ChemSampCo, Inc.
Tel
--
Fax
--
Email
sales@chemsampco.com
Country
United States
ProdList
3585
Advantage
60
Leonid Chemicals Private Limited
Tel
--
Fax
--
Email
careers@leonidchemicals.com
Country
United States
ProdList
1700
Advantage
43
Naugra Export
Tel
--
Fax
--
Country
United States
ProdList
1332
Advantage
47
2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
API, Inc.
Tel
--
Fax
--
Email
HenryNiemczyk@apiincnj.com
Country
United States
ProdList
118
Advantage
30
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
SKC Inc.
Tel
--
Fax
--
Email
skcorder@skcinc.com
Country
United States
ProdList
1378
Advantage
76
Parchem Trading Ltd.
Tel
--
Fax
--
Email
info@par-chem.com
Country
United States
ProdList
740
Advantage
66
Parchem Trading Ltd.
Tel
--
Fax
--
Email
info@parchem.com
Country
United States
ProdList
794
Advantage
76
Sciencelab.com, Inc.
Tel
--
Fax
--
Email
accounting@sciencelab.com
Country
United States
ProdList
4159
Advantage
82
Loba Chemie Pvt. Ltd.
Tel
--
Fax
--
Country
United States
ProdList
1945
Advantage
71
City Chemical LLC
Tel
--
Fax
--
Email
sales@citychemical.com
Country
United States
ProdList
6708
Advantage
72
Pfaltz & Bauer, Inc.
Tel
--
Fax
--
Email
sales@pfaltzandbauer.com
Country
United States
ProdList
6828
Advantage
72
Monomer-Polymer & Dajac Laboratories, Inc.
Tel
--
Fax
--
Email
monomerpolymer@comcast.net
Country
United States
ProdList
1989
Advantage
60
More
Less

View Lastest Price from Isophthalic acid manufacturers

Hebei Saisier Technology Co., LTD
Product
Isophthalic acid 121-91-5
Price
US $6.00/KG
Min. Order
1KG
Purity
More than 99%
Supply Ability
2000KG/Month
Release date
2024-04-25
Hebei Mujin Biotechnology Co.,Ltd
Product
Isophthalic acid 121-91-5
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-06-25
Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
Isophthalic acid 121-91-5
Price
US $60.00/kg
Min. Order
1kg
Purity
99
Supply Ability
5000
Release date
2024-05-15

121-91-5, Isophthalic acidRelated Search:


  • RARECHEM AL BO 0036
  • M-PHTHALIC ACID
  • 1,3-dicarboxybenzene
  • 1,3-phthalicacid
  • m-benzenedicarboxylicacid
  • m-Dicarboxybenzene
  • 1,3-BENZENEDICARBOXYLIC ACID
  • 1,3-PHENYL DICARBOXYLIC ACID
  • ISOPHTHALIC ACID
  • Isophthalic Acid/Benzene-1,3-dicarboxylic acid(IPA)
  • IsophthalicAcidForSynthesis
  • ISOPHTHALIC ACID (M-PHTHALIC ACID )
  • Isophthalic
  • Isophthalic acid reference substance
  • META-PHTHALICACID
  • BENZENE-1,3-DICARBOXYLIC ACID / ISOPHTHALIC ACID
  • Isophthalic acid -Respirable Dust
  • Isophthalic acid Total Dust
  • ISOPHTHALIC ACID pure
  • Isophthalic acid,99%
  • PIA Benzene-1,3-dicarboxylic acid
  • Acide isophtalique
  • acideisophtalique
  • acideisophtalique(french)
  • isophthalate
  • Kyselina isoftalova
  • kyselinaisoftalova
  • kyselinaisoftalova(czech)
  • m-Benzenedicarboxylic acid
  • Benzene-M-dicarboxylic acid
  • Isophthalic acid, 99% 2KG
  • Isophthalic acid, 99% 5GR
  • Isophthalic acid, synthesis grade
  • IPA)Isophthalic
  • Isophthalic acid (IPA)
  • Isophthalic acid 99%
  • Benzene-1,3-dicarboxylic aci
  • Isophthalic acid, 99.5%
  • Isophthalic acid(PIA)
  • IsophthalicAcidSolution,100mg/L,1ml
  • IsophthalicAcid&gt
  • Isophthalic acid, 99.5%, for synthesis
  • sophthalic acid
  • M-Phthalic Acid Pia
  • Indobufen Impurity 51
  • C14447000 IsophthaliCacid
  • Bexagliflozin Impurity 7
  • 2-(4-aminophenyl)butanehydrazide
  • 121-91-5
  • 121915
  • HOOCC6H4COOH
  • C6H413CO2H2
  • Organic Building Blocks
  • Carboxylic Acids
  • Carbonyl Compounds
  • C8
  • Building Blocks
  • solvents and intermediates