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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
EC Number:
214-527-0
MDL number:
MFCD00004105
UNSPSC Code:
12352100
PubChem Substance ID:
24874368
NACRES:
NA.22

Key Documents

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Quality Level

100

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
15021MU

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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)
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)
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
Synthesis methods for 2, 6-naphthalenedicarboxylic acid
Elman AR
Catalysis in Industry, 1(3), 184-184 (2009)
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