ChemicalBook >> CAS DataBase List >>Phthalic acid

Phthalic acid

CAS No.
88-99-3
Chemical Name:
Phthalic acid
Synonyms
1,2-BENZENEDICARBOXYLIC ACID;O-PHTHALIC ACID;BENZENE-1,2-DICARBOXYLIC ACID;Phthalic acid,99%;Fluorescein EP Impurity B;NSC 5348;Phthalsure;Sunftal 20;THALIC ACID;phthalicaci
CBNumber:
CB6289456
Molecular Formula:
C8H6O4
Molecular Weight:
166.13
MDL Number:
MFCD00002467
MOL File:
88-99-3.mol
MSDS File:
SDS
Last updated:2025-09-30 18:11:34

Phthalic acid Properties

Melting point 210-211 °C (dec.) (lit.)
Boiling point 214.32°C (rough estimate)
Density 1.59 g/cm3 at 15 °C
bulk density 960kg/m3
vapor pressure 7.8 hPa (191 °C)
refractive index 1.5100 (estimate)
Flash point 168 °C
storage temp. Store below +30°C.
solubility methanol: 0.1 g/mL, clear
pka 2.89(at 25℃)
form Powder
color White
PH 3.2(1 mM solution);2.55(10 mM solution);2(100 mM solution);
Water Solubility 7 g/L (25 ºC)
Merck 14,7371
BRN 608199
Dielectric constant 5.1(Ambient)
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey XNGIFLGASWRNHJ-UHFFFAOYSA-N
LogP 0.73 at 20℃
Indirect Additives used in Food Contact Substances O-PHTHALIC ACID
FDA 21 CFR 175.105
CAS DataBase Reference 88-99-3(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 6O7F7IX66E
NIST Chemistry Reference 1,2-Benzenedicarboxylic acid(88-99-3)
EPA Substance Registry System Phthalic acid (88-99-3)
UNSPSC Code 85151701
NACRES NA.24

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  26-36-37/39
WGK Germany  1
RTECS  TH9625000
TSCA  Yes
HS Code  29173980
Hazardous Substances Data 88-99-3(Hazardous Substances Data)
Toxicity LD50 orally in rats: 7.9 g/kg (Shaffer)
NFPA 704
1
1 0

Phthalic acid price More Price(45)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0000766 Phthalic acid European Pharmacopoeia (EP) Reference Standard 88-99-3 20 mg $118 2025-07-31 Buy
Sigma-Aldrich 8.22298 Phthalic acid for synthesis 88-99-3 100g $45.5 2025-07-31 Buy
Sigma-Aldrich 8.22298 Phthalic acid for synthesis 88-99-3 1kg $180 2025-07-31 Buy
Sigma-Aldrich 402915 Phthalic acid ACS reagent, ≥99.5% 88-99-3 1kg $111 2025-07-31 Buy
Sigma-Aldrich 1535899 Phthalic acid United States Pharmacopeia (USP) Reference Standard 88-99-3 50mg $442 2025-07-31 Buy
Product number Packaging Price Buy
Y0000766 20 mg $118 Buy
8.22298 100g $45.5 Buy
8.22298 1kg $180 Buy
402915 1kg $111 Buy
1535899 50mg $442 Buy

Phthalic acid Chemical Properties,Uses,Production

Description

Phthalic acid is an aromatic dicarboxylic acid, with formula C6H4(CO2H)2. It is an isomer of isophthalic acid and terephthalic acid. Although phthalic acid is of modest commercial importance, the closely related derivative phthalic anhydride is a commodity chemical produced on a large scale.

Chemical Properties

PHTHALIC ACID,C6H4(COOH)2, mp 208 °C (ortho), 330 °C (meta and iso), the ortho form sublimes and the meta and iso forms decompose with heat, sp gr 1.593 (ortho). Phthalic acid is very slightly soluble in H2O, soluble in alcohol, and slightly soluble in ether. The solid form is colorless, crystalline

Uses

It is a dibasic acid, with pKa's of 2.89 and 5.51. The mono potassium salt, potassium hydrogen phthalate is a standard acid in analytical chemistry. Typically phthalate esters are prepared from the widely available phthalic anhydride. Reduction of phthalic acid with sodium amalgam in the presence of water gives the 1,3- cyclohexadiene derivative.

Uses

Phthalic Acid (Phenyl-13C6, D4) is labelled Phthalic Acid (P384480) which is an organic reagent used to synthesize phthalates.

Definition

ChEBI: Phthalic acid is a benzenedicarboxylic acid cosisting of two carboxy groups at ortho positions. It has a role as a human xenobiotic metabolite. It is a conjugate acid of a phthalate(1-).

Production Methods

Phthalic acid is produced by the catalytic oxidation of naphthalene directly to phthalic anhydride and a subsequent hydrolysis of the anhydride.
Phthalic acid was first obtained by French chemist Auguste Laurent in 1836 by oxidizing naphthalene tetrachloride. Believing the resulting substance to be a naphthalene derivative, he named it "naphthalic acid". After the Swiss chemist Jean Charles Galissard de Marignac determined its correct formula, Laurent gave it its present name. Manufacturing methods in the nineteenth century included oxidation of naphthalene tetrachloride with nitric acid, or, better, oxidation of the hydrocarbon with fuming sulfuric acid, using mercury or mercury(II) sulfate as a catalyst.

Definition

phthalic acid: colourlesscrystalline dicarboxylic acid,C6H4(COOH)2; r.d. 1.6; m.p. 207°C.The two –COOH groups are substitutedon adjacent carbon atoms ofthe ring, the technical name beingbenzene-1,2-dicarboxylic acid. Theacid is made from phthalic anhydride(benzene-1,2-dicarboxylic anhydride,C8H4O3), which is made by the catalyticoxidation of naphthalene. Theanhydride is used in making plasticizersand polyester resins.

Synthesis Reference(s)

The Journal of Organic Chemistry, 30, p. 2414, 1965 DOI: 10.1021/jo01018a074

General Description

White crystals or fine white powder.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Phthalic acid is a carboxylic acid. Phthalic acid is sensitive to exposure to extreme heat. Phthalic acid reacts violently with nitric acid. Phthalic acid is incompatible with sodium nitrite. Phthalic acid is also incompatible with oxidizers. .

Fire Hazard

Phthalic acid is combustible.

Flammability and Explosibility

Not classified

Safety Profile

Moderately toxic by ingestion and intraperitoneal routes. A skin and mucous membrane irritant. Combustible when heated. In the form of dust (anhydride) it can explode. Mixtures with sodmm nitrite explode when heated. Violent reaction with HNO3. When heated to decomposition it emits acrid smoke and irritating fumes. Used in synthesis of dyes and dyestuffs, in medcines and perfumes.

Safety

The toxicity of phthalic acid is low with LD50 (mouse) of 550 mg/kg. However, many phthalate esters have been implicated as endocrine disruptors.

Purification Methods

Crystallise phthalic acid from water. [Beilstein 9 IV 3167.]

Isomers

Phthalic acid is one of three isomers of benzene dicarboxylic acid, the others being iso phthalic acid and terephthalic acid. Sometimes the term "phthalic acids" is used to refer to this family of isomers, but in the singular, "phthalic acid", refers exclusively to the ortho- isomer.

Global( 583)Suppliers
Supplier Tel Email Country ProdList Advantage
ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
+86-13017695106 +86-13676922317 jiuyitime@fdachem.com China 9029 58
Hebei Chuanghai Biotechnology Co., Ltd
+8617732866630 abby@chuanghaibio.com China 8773 58
Hebei Chuanghai Biotechnology Co,.LTD
+86-13131129325 sales1@chuanghaibio.com China 5251 58
Anhui Ruihan Technology Co., Ltd
+8617756083858 daisy@anhuiruihan.com China 973 58
airuikechemical co., ltd.
+86-18353166132 sales02@airuikechemical.com China 983 58
Hebei Zhuanglai Chemical Trading Co.,Ltd
+8613343047651 admin@zlchemi.com China 3692 58
Capot Chemical Co.,Ltd.
+8613336195806 sales@capot.com China 29734 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21620 55
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +8618949832763 info@tnjchem.com China 2988 55
Shanghai Zheyan Biotech Co., Ltd.
18017610038 zheyansh@163.com CHINA 3619 58

View Lastest Price from Phthalic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Phthalic acid pictures 2025-09-30 Phthalic acid
88-99-3
US $48.00 / g 98.00% 10g TargetMol Chemicals Inc.
Butyphthalide impurity 23 pictures 2025-09-25 Butyphthalide impurity 23
88-99-3
US $0.00-0.00 / mg 10mg 0.98 5g ShenZhen H&D Pharmaceutical Technology Co., LTD
Phthalic Acid pictures 2025-09-25 Phthalic Acid
US $0.00-0.00 / mg 10mg 0.98 5g ShenZhen H&D Pharmaceutical Technology Co., LTD
  • Phthalic Acid pictures
  • Phthalic Acid
  • US $0.00-0.00 / mg
  • 0.98
  • ShenZhen H&D Pharmaceutical Technology Co., LTD
1,2-dicarboxybenzene 1,2-phthalicacid Acide phtalique acidephtalique acidephtalique(french) Kyselina ftalova kyselinaftalova o-Benzenedicarboxylic acid Phthalate Ion Chromatography Standard Solution Fluka PHTHALIC ACID, 1000MG, NEAT PHTHALIC ACID ACS REAGENT PHTHALIC ACID REAGENT GRADE 98% PATHALIC ACID PhthalicAcidAcs PhthalicAcidGr99.5% PhthalicAcidForSynthesis ORTHO-PHTHALICACIDANDITSSODIUMANDPOTASSIUMSALTS Phthalsure O-PHTHALIC ACID (PHTHALIC ACID ) Phthalic acid, 99.5% PHTHALIC ACID REAGENT (ACS) BENZENE-1,2-DICARBOXYLIC ACID / O-PHTHALIC ACID Phthalic acid, ACS, 99.5+% PHTHALIC ACID PURE 1,2-Benzenedicarboxylic acid, Phthalic acid Phthalate standard for IC Phthalic acid,99% THALIC ACID Phthalic acid, 99% 1KG Phthalic acid, 99% 250GR NSC 5348 Butyphthalide impurity 23 PHTHALIC ACID, REAGENT (ACS)PHTHALIC ACID, REAGENT (ACS)PHTHALIC ACID, REAGENT (ACS)PHTHALIC ACID, REAGENT (ACS) o-benzenedicarboxylicacid Sunftal 20 BENZENE-1,2-DICARBOXYLIC ACID AURORA 15195 DIISONOYL PHTHALATE (DINP) PHTHALIC ACID, 99.5+%, A.C.S. REAGENT o-Carboxybenzoic Acid RARECHEM AL BO 0013 PHTHALATE ION CHROMATOGRAPHY STANDARD PHTHALIC ACID ORTHO-PHTHALIC ACID O-PHTHALIC ACID O-DICARBOXYBENZENE 1,2-BENZENEDICARBONXYLIC ACID 1,2-BENZENEDICARBONIC ACID, ANHYDRIDE 1,2-BENZENEDICARBOXYLIC ACID 1,2-PHENYL DICARBOXYLIC ACID Phthalic acid ACS reagent, >=99.5% Phthalic acid puriss. p.a., >=99.5% (T) Phthalic acid reagent grade, 98% Phthalic acid Vetec(TM) reagent grade, 98% TOTALBLOT+ PVDF MEMBRANES 0-Phthalic acid Phthalic acid, ACS, 99.5% min. Phthalic acid, For ACS analysis