ChemicalBook > CAS DataBase List > 2,6-NAPHTHALENEDICARBOXYLIC ACID

2,6-NAPHTHALENEDICARBOXYLIC ACID

Product Name
2,6-NAPHTHALENEDICARBOXYLIC ACID
CAS No.
1141-38-4
Chemical Name
2,6-NAPHTHALENEDICARBOXYLIC ACID
Synonyms
NAPHTHALENE-2,6-DICARBOXYLIC ACID;2,6-NAPHTHALIC ACID;2,6-NAPTHALENEDICARBOXYLIC ACID;DK7461;NSC 96410;JACS-1141-38-4;TIMTEC-BB SBB008377;Adiphenine Impurity 11;2,6-Naphthalenedioic acid;2,6-phthalenedicarboxylic Acid
CBNumber
CB9215403
Molecular Formula
C12H8O4
Formula Weight
216.19
MOL File
1141-38-4.mol
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2,6-NAPHTHALENEDICARBOXYLIC ACID Property

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
pka
3.69±0.30(Predicted)
form 
Powder
color 
white
Water Solubility 
3μg/L at 20℃
BRN 
2051257
InChI
InChI=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)
InChIKey
RXOHFPCZGPKIRD-UHFFFAOYSA-N
SMILES
C1=C2C(C=C(C(O)=O)C=C2)=CC=C1C(O)=O
LogP
2.22
CAS DataBase Reference
1141-38-4(CAS DataBase Reference)
EPA Substance Registry System
2,6-Naphthalenedicarboxylic acid (1141-38-4)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
24/25
WGK Germany 
3
TSCA 
T
HazardClass 
IRRITANT
HS Code 
29173990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

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

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
301353
Product name
2,6-Naphthalenedicarboxylic acid
Purity
95%
Packaging
5g
Price
$65.07
Updated
2025/07/31
Sigma-Aldrich
Product number
301353
Product name
2,6-Naphthalenedicarboxylic acid
Purity
95%
Packaging
25g
Price
$128.25
Updated
2025/07/31
TCI Chemical
Product number
N0377
Product name
2,6-Naphthalenedicarboxylic Acid
Purity
>98.0%(GC)(T)
Packaging
5g
Price
$39
Updated
2025/07/31
TCI Chemical
Product number
N0377
Product name
2,6-Naphthalenedicarboxylic Acid
Purity
>98.0%(GC)(T)
Packaging
25g
Price
$115
Updated
2025/07/31
Strem Chemicals
Product number
08-1235
Product name
2,6-Naphthalenedicarboxylic acid, min. 98%
Packaging
5g
Price
$55
Updated
2024/03/01
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2,6-NAPHTHALENEDICARBOXYLIC ACID Chemical Properties,Usage,Production

Chemical Properties

BEIGE POWDER

Uses

2,6-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.

Uses

2,6-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.

Uses

A polybasic acid intended for use as components of resinous and polymeric coatings that contact food.

Definition

ChEBI: Naphthalene-2,6-dicarboxylic acid is a dicarboxylic acid. It derives from a hydride of a naphthalene.

General Description

This product has been enhanced for energy efficiency.

Flammability and Explosibility

Not classified

Synthesis

2,6-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:

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.

2,6-NAPHTHALENEDICARBOXYLIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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2,6-NAPHTHALENEDICARBOXYLIC ACID Suppliers

Aladdin Scientific
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View Lastest Price from 2,6-NAPHTHALENEDICARBOXYLIC ACID manufacturers

Shaanxi Dideu New Materials Co. Ltd
Product
2,6-NAPHTHALENEDICARBOXYLIC ACID 1141-38-4
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98.0%
Supply Ability
10000KGS
Release date
2025-05-19
Henan Aochuang Chemical Co.,Ltd.
Product
2,6-NAPHTHALENEDICARBOXYLIC ACID 1141-38-4
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1ton
Release date
2022-09-28
Hebei Chuanghai Biotechnology Co,.LTD
Product
2, 6-Naphthalenedicarboxylic Acid 1141-38-4
Price
US $5.00-2.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10000kg
Release date
2024-08-15

1141-38-4, 2,6-NAPHTHALENEDICARBOXYLIC ACIDRelated Search:


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  • Adiphenine Impurity 11
  • 2,6-Naphthalenedioic acid
  • 2,6-phthalenedicarboxylic Acid
  • 1141-38-4
  • C11 to C12
  • Carboxylic Acids
  • Carbonyl Compounds
  • Organic Building Blocks
  • Building Blocks
  • 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