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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;Naphthaline-2,6-dicarbonic acid;2,6-NAPHTHALENEDICARBOXYLIC ACID
CBNumber:
CB9215403
Molecular Formula:
C12H8O4
Molecular Weight:
216.19
MDL Number:
MFCD00004105
MOL File:
1141-38-4.mol
MSDS File:
SDS
Last updated:2025-04-29 17:45:46

2,6-NAPHTHALENEDICARBOXYLIC ACID 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
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
Indirect Additives used in Food Contact Substances 2,6-NAPHTHALENEDICARBOXYLIC ACID
CAS DataBase Reference 1141-38-4(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII K3C4DYZ29O
EPA Substance Registry System 2,6-Naphthalenedicarboxylic acid (1141-38-4)
UNSPSC Code 12352106
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  24/25
WGK Germany  3
TSCA  T
HazardClass  IRRITANT
HS Code  29173990
NFPA 704
0
0 0

2,6-NAPHTHALENEDICARBOXYLIC ACID price More Price(35)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 301353 2,6-Naphthalenedicarboxylic acid 95% 1141-38-4 25g $52.4 2024-03-01 Buy
Sigma-Aldrich 301353 2,6-Naphthalenedicarboxylic acid 95% 1141-38-4 5g $66.5 2024-03-01 Buy
TCI Chemical N0377 2,6-Naphthalenedicarboxylic Acid >98.0%(GC)(T) 1141-38-4 5g $39 2024-03-01 Buy
TCI Chemical N0377 2,6-Naphthalenedicarboxylic Acid >98.0%(GC)(T) 1141-38-4 25g $115 2024-03-01 Buy
Alfa Aesar A16868 Naphthalene-2,6-dicarboxylic acid, 98+% 1141-38-4 5g $58.1 2024-03-01 Buy
Product number Packaging Price Buy
301353 25g $52.4 Buy
301353 5g $66.5 Buy
N0377 5g $39 Buy
N0377 25g $115 Buy
A16868 5g $58.1 Buy

2,6-NAPHTHALENEDICARBOXYLIC ACID Chemical Properties,Uses,Production

Chemical Properties

BEIGE POWDER

Uses

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

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.

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:
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.

581-42-0
1141-38-4
Synthesis of 2,6-NAPHTHALENEDICARBOXYLIC ACID from 2,6-DIMETHYLNAPHTHALENE
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View Lastest Price from 2,6-NAPHTHALENEDICARBOXYLIC ACID manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,6-Naphthalenedicarboxylic acid pictures 2025-05-13 2,6-Naphthalenedicarboxylic acid
1141-38-4
0.99 RongNa Biotechnology Co.,Ltd
2,6-NAPHTHALENEDICARBOXYLIC ACID pictures 2025-05-12 2,6-NAPHTHALENEDICARBOXYLIC ACID
1141-38-4
US $0.00 / kg 1kg 99% 10000KGS Shaanxi Dideu New Materials Co. Ltd
2,6-NAPHTHALENEDICARBOXYLIC ACID pictures 2025-04-04 2,6-NAPHTHALENEDICARBOXYLIC ACID
1141-38-4
US $0.00-0.00 / KG 1KG 98% 1ton Henan Aochuang Chemical Co.,Ltd.
NAPHTHALENE-2,6-DICARBOXYLIC ACID 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 2,6-Naphthalenedicarboxylic acid,97% Naphthaline-2,6-dicarbonic acid NSC 96410 2,6-Naphthalenedicarboxylic acid 99% 2,6-Naphthalenedicarboxylic acid, min. 98% 2,6-Naphthalenedicarboxylic acid,neat,neat JACS-1141-38-4 2,6-NaphthalenedicarboxylicAcid> DK7461 2,6-Naphthalenedicarboxylic acid (8CI, 9CI, ACI) Adiphenine Impurity 11 2,6-Naphthalenedicarboxylic Acid, ≥ 98.0% 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