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523763

Sigma-Aldrich

2,6-Naphthalenedicarboxylic acid

greener alternative

99%

Sinónimos:

2,6-Naphthalic acid

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About This Item

Fórmula lineal:
C10H6(CO2H)2
Número de CAS:
1141-38-4
Peso molecular:
216.19
EC Number:
214-527-0
MDL number:
MFCD00004105
UNSPSC Code:
12352100
PubChem Substance ID:
24874368
NACRES:
NA.22

assay

99%

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

mp

>300 °C (lit.)

functional group

carboxylic acid

greener alternative category

, Enabling

SMILES string

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

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)

InChI key

RXOHFPCZGPKIRD-UHFFFAOYSA-N

Gene Information

human ... PTPN1(5770)

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General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

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.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (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)
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
Ewa Dabek-Zlotorzynska et al.
Methods in molecular biology (Clifton, N.J.), 384, 43-64 (2008-04-09)
Within the last few years, capillary electrophoresis (CE), especially with indirect ultraviolet detection, has successfully been utilized for the analysis of low-molecular-weight (LMW) organic acids in a wide variety of matrices (e.g., food, pharmaceutical, environmental, industrial, clinical). The speed, resolution
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