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Merck
모든 사진(2)

주요 문서

523763

Sigma-Aldrich

2,6-Naphthalenedicarboxylic acid

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99%

동의어(들):

2,6-Naphthalic acid

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About This Item

Linear Formula:
C10H6(CO2H)2
CAS Number:
Molecular Weight:
216.19
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

99%

환경친화적 대안 제품 특성

Design for Energy Efficiency
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sustainability

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mp

>300 °C (lit.)

작용기

carboxylic acid

환경친화적 대안 카테고리

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

유전자 정보

human ... PTPN1(5770)

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애플리케이션

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

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

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

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