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2,6-NAPHTHALENEDICARBOXYLIC ACID

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Company Name: Shanghai Daken Advanced Materials Co.,Ltd
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Products Intro: Product Name:2,6-NAPHTHALENEDICARBOXYLIC ACID
CAS:1141-38-4
Purity:0.99 Package:5KG;1KG
Company Name: Shaanxi Dideu Medichem Co. Ltd
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Products Intro: Product Name:2,6-Naphthalenedicarboxylic Acid
CAS:1141-38-4
Purity:99.0% Package:1KG;0.00;USD|25KG;0.00;USD|200KG;0.00;USD
Company Name: Hebei Chuanghai Biotechnology Co,.LTD
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Products Intro: Product Name:2, 6-Naphthalenedicarboxylic Acid
CAS:1141-38-4
Purity:99% Package:1KG;5.00;USD|10KG;3.00;USD|50KG;2.00;USD
Company Name: Henan Fengda Chemical Co., Ltd
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Products Intro: Product Name:2,6-Naphthalenedicarboxylic acid
CAS:1141-38-4
Purity:99%, 99.5% Sublimated Package:1KG;200USD|100KG;1USD
Company Name: Capot Chemical Co.,Ltd.
Tel: +86-(0)57185586718; +8613336195806
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Products Intro: Product Name:2,6-Naphthalenedicarboxylic acid
CAS:1141-38-4
Purity:98% Min. Package:1G;1KG;100KG

2,6-NAPHTHALENEDICARBOXYLIC ACID manufacturers

2,6-NAPHTHALENEDICARBOXYLIC ACID Basic information
Product Name:2,6-NAPHTHALENEDICARBOXYLIC ACID
Synonyms:TIMTEC-BB SBB008377;2,6-NAPHTHALENEDICARBOXYLIC ACID;2,6-NAPHTHALIC ACID;2,6-NAPHTHALENEDICARBOXYLIC ACID, 99.5+%;2,6-NAPHTHALENEDICARBOXYLIC ACID 98+%;Naphthalene-2,6-dicarboxylic acid, 98+%;Naphthalene-2,6-dicarboxylic acid 99%;2,6-NAPTHALENEDICARBOXYLIC ACID
CAS:1141-38-4
MF:C12H8O4
MW:216.19
EINECS:214-527-0
Product Categories:Achiral Oxygen;Naphthalene derivatives;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Carboxylic Acid MonomersAlternative Energy;Physisorption;Materials for Hydrogen Storage;Monomers;Polymer Science;C11 to C12;Carbonyl Compounds;Carboxylic Acids;Intermediates of Dyes and Pigments
Mol File:1141-38-4.mol
2,6-NAPHTHALENEDICARBOXYLIC ACID Structure
2,6-NAPHTHALENEDICARBOXYLIC ACID Chemical Properties
Melting point >300 °C (lit.)
Boiling point 316.6°C (rough estimate)
density 1.5
refractive index 1.7080 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility very faint turbidity in hot Pyridine
pka3.69±0.30(Predicted)
form Powder
color white
Water Solubility 3μg/L at 20℃
BRN 2051257
InChIInChI=1S/C12H8O4/c13-11(14)9-3-1-7-5-10(12(15)16)4-2-8(7)6-9/h1-6H,(H,13,14)(H,15,16)
InChIKeyRXOHFPCZGPKIRD-UHFFFAOYSA-N
SMILESC1=C2C(C=C(C(O)=O)C=C2)=CC=C1C(O)=O
LogP2.22
CAS DataBase Reference1141-38-4(CAS DataBase Reference)
EPA Substance Registry System2,6-Naphthalenedicarboxylic acid (1141-38-4)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 24/25
WGK Germany 3
TSCA TSCA listed
HazardClass IRRITANT
HS Code 29173990
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
2,6-NAPHTHALENEDICARBOXYLIC ACID Usage And Synthesis
Chemical PropertiesBEIGE POWDER
UsesA polybasic acid intended for use as components of resinous and polymeric coatings that contact food.
Uses2,6-naphthalenedicarboxylic acid is an important product for the manufacture of high strength and excellent dyeing properties of polyester fibers and F class insulation material, is an important monomer performance PEN, PBN, liquid crystal polymer (LCP) and polyurethane resin pharmaceutical and fine chemicals raw material.
Uses2,6-Naphthalenedicarboxylic acid (H2ndc) can be used in the formation of metal-organic coordination polymers (MOCPs) for potential applications in various fields such as adsorption, separation, and magnetism. It can also be used as a monomer in the production of polyesters. H2ndc can also be used in the synthesis of a metal-organic framework (MOF), which can further be used as a drug carrier.
DefinitionChEBI: Naphthalene-2,6-dicarboxylic acid is a dicarboxylic acid. It derives from a hydride of a naphthalene.
General DescriptionThis product has been enhanced for energy efficiency.
Flammability and ExplosibilityNot classified
Synthesis2,6-Naphthalenedicarboxylic acid (2,6-NDA) is selectively synthesized from 2-naphthoic acid (2-NCA) and carbon tetrachloride in aqueous sodium hydroxide solution under mild conditions using cyclodextrin (β-CyD) as a catalyst[1]. The specific reaction steps are as follows:
2,6-NAPHTHALENEDICARBOXYLIC ACID synthesis
Three mmol of 2-naphthalenecarboxylic acid/2-NCA), 0,8 mmol(0,05 g) of copper powder, and 3,0 mmol of β-CyD were added to 30 mL of 30 wt.-% aqueous sodium hydroxide solution. The reaction was started with the addition of 8,5 mmol of carbon tetrachloride and was continued at 60°C for 7 h with magnetic stirring under nitrogen. Then, the residual carbon tetrachloride was removed by evaporation under reduced pressure.
References[1] HIDEFUMI HIRAI; Rikinori T; Hisashi Mihori. Selective synthesis of 2,6-naphthalenedicarboxylic acid using cyclodextrin as catalyst[J]. Macromolecular Rapid Communications, 1993, 14 7: 439-443. DOI:10.1002/marc.1993.030140712.
Tag:2,6-NAPHTHALENEDICARBOXYLIC ACID(1141-38-4) Related Product Information
2,3-Naphthalenedicarboxylic acid 1,4-NAPHTHALENEDICARBOXYLIC ACID 95+%,1,4-NAPHTHALENEDICARBOXYLIC ACID Disodium 1,5-naphthalenedisulfonate NAPHTHALENE 1,4-DICARBOXALDEHYDE 1,4-DIAMINONAPHTHALENE 2,3-diaminonaphthalene Dimethyl ester of 2,6-naphthalenedicarboxylic acid,2,6-NAPHTHALENEDICARBOXYLIC ACID DIMETHYL ESTER,2,6-NAPHTHALENEDICARBOXYLIC ACID DIMETHYL ESTER 99+% 2,6-NAPHTHALENEDICARBOXYLIC ACID 2,3-NAPHTHALENEDICARBOXYLIC ACID DIMETHYL ESTER Diundecyl phthalate 2,7-NAPHTHALENEDICARBOXYLIC ACID 1,8-NAPHTHALENEDICARBOXYLIC ACID ANHYDRIDE 3-Hydroxy-1,8-naphthalic anhydride 2,7-NAPHTHALENEDICARBOXYLIC ACID DIMETHYL ESTER 3-HYDROXY-2,7-NAPHTHALENEDICARBOXYLIC ACID 2,6-naphthalenedicarboxylic acid, monomethyl ester 2,6-NAPHTHALENEDICARBOXYLIC ACID, DIPOTASSIUM SALT 6-(ETHOXYCARBONYL)-2-NAPHTHOIC ACID