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Merck
CN

523763

2,6-Naphthalenedicarboxylic acid

greener alternative

99%

Synonym(s):

2,6-Naphthalic acid

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About This Item

Linear Formula:
C10H6(CO2H)2
CAS Number:
1141-38-4
Molecular Weight:
216.19
NACRES:
NA.22
PubChem Substance ID:
24874368
UNSPSC Code:
12352100
EC Number:
214-527-0
MDL number:
MFCD00004105

Key Documents

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Product Name

2,6-Naphthalenedicarboxylic acid, 99%

InChI key

RXOHFPCZGPKIRD-UHFFFAOYSA-N

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)

SMILES string

OC(=O)c1ccc2cc(ccc2c1)C(O)=O

assay

99%

greener alternative product characteristics

Design for Energy Efficiency
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sustainability

Greener Alternative Product

mp

>300 °C (lit.)

functional group

carboxylic acid

greener alternative category

, Enabling

Quality Level

100

Gene Information

human ... PTPN1(5770)

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Application

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.

General description

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
15021MU

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Structural modulation and properties of silver (I) coordination polymers from 2, 6-naphthalenedicarboxylic acid and flexible N-donor linkers
Wang XX, et al.
Transition Metal Chemistry, 40(7), 733-742 (2015)
Synthesis of metal-organic framework from iron nitrate and 2, 6-naphthalenedicarboxylic acid and its application as drug carrier
Ibrahim M, et al.
Journal of Nanoscience and Nanotechnology, 18(8), 5266-5273 (2018)
Vladimir Setnicka et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 58(13), 2983-2989 (2002-12-13)
The host/guest complexation between cyclodextrins (CDs) and aromatic compounds was studied by vibrational circular dichroism (VCD) spectroscopy in mid-IR region. Benzoic acid, 4-aminobenzoic acid, and 2,6-naphthalene-dicarboxylic acid acting as the guests with aromatic skeleton, cause the significant changes in VCD
M A Strege et al.
Journal of chromatography. B, Biomedical sciences and applications, 697(1-2), 255-257 (1997-10-29)
A rapid and simple method for the capillary electrophoretic determination of residual trifluoroacetic acid in lyophilized natural products is described. The technique utilizes 2,6-naphthalenedicarboxylic acid as a separation buffer additive providing indirect ultraviolet absorption detection. Using this method, acceptable precision
Dong-Sung Kim et al.
Biotechnology letters, 30(2), 329-333 (2007-10-05)
Crude 2,6-naphthalene dicarboxylic acid was purified by Pseudomonas sp. HN-72 which biotransformed the major impurity of 2-formyl-6-naphthoic acid into 2,6-naphthalene dicarboxylic acid. The biotransformation yield reached 100% when the reaction was performed at 40 degrees C for 1 h, in
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