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Catalog Number:
47439
CAS Number:
7149-49-7
2,3-Naphtalènedialdéhyde
Purity:
≥ 99% (GC)
Synonym(s):
NDA
Documents
$135.60 /100 mg
Taille
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Product Information

Le 2,3-naphtalènedialdéhyde est utilisé comme agent de marquage fluorescent pour la quantification de l'histamine dans les préparations d'immunoglobulines humaines

Synonyms
NDA
CAS Number
7149-49-7
Purity
≥ 99% (GC)
Molecular Formula
C12H8O2
Molecular Weight
184.19
MDL Number
MFCD00016618
PubChem ID
96400
Melting Point
131 - 135 °C
Appearance
Poudre blanche à jaune pâle
Optical Rotation
[a]20/D = 42 - 45 ° (C=0,2 dans le chloroforme)
Conditions
Conserver entre 2 et 8 °C, sous gaz inerte.
General Information
Synonyms
NDA
CAS Number
7149-49-7
Purity
≥ 99% (GC)
Molecular Formula
C12H8O2
Molecular Weight
184.19
MDL Number
MFCD00016618
PubChem ID
96400
Melting Point
131 - 135 °C
Appearance
Poudre blanche à jaune pâle
Optical Rotation
[a]20/D = 42 - 45 ° (C=0,2 dans le chloroforme)
Conditions
Conserver entre 2 et 8 °C, sous gaz inerte.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2,3-Naphthalenedialdehyde is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, enabling the synthesis of complex molecules and materials, which is crucial for developing new pharmaceuticals and agrochemicals.
  • Fluorescent Dyes: Its unique structure allows it to be used in the production of fluorescent dyes, which are essential in biological imaging and diagnostics, enhancing visibility in various applications.
  • Polymer Chemistry: 2,3-Naphthalenedialdehyde is employed in the synthesis of specialized polymers, improving properties such as thermal stability and mechanical strength, making it valuable in the manufacturing of high-performance materials.
  • Biological Research: The compound is utilized in studies related to enzyme inhibition and protein interactions, offering insights into biochemical pathways and potential therapeutic targets.
  • Antimicrobial Agents: Its derivatives have shown promise as antimicrobial agents, providing a basis for developing new treatments against resistant strains of bacteria and fungi.

Citations