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Cat. No.: HY-Y0075S1

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2-Naphthaldehyde-¹³C

2-Naphthaldehyde-13C is the ¹³C-labeled 2-Naphthaldehyde (HY-Y0075). 2-Naphthaldehyde belongs to naphthalene-based bis-aromatic aldehyde compounds. 2-Naphthaldehyde scavenges DPPH and ABTS⁺ free radicals, and exerts reductive effects by donating hydrogen atoms to interrupt free radical chain reactions. 2-Naphthaldehyde inhibits the growth and proliferation of colon cancer cells. 2-Naphthaldehyde serves as a substrate for NAD⁺-dependent salicylaldehyde dehydrogenase from Pseudomonas strain C6 and is catalytically oxidized. 2-Naphthaldehyde acts as a precursor material for the chemical synthesis of antioxidant Schiff bases.

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CAS No.: 116815-49-7
Formule: C₁₀¹³CH₈O
Masse moléculaire:157.17

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Please store the product under the recommended conditions in the Certificate of Analysis.

2-Naphthaldehyde-¹³C Chemical Structure

CAS No.: 116815-49-7

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Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Activité biologique
- Description
- Application
Chemical Information
Protocole (1)
Pureté et documentation
Références
Calculators
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Activité biologique

Description

Application

1. This compound can be used as a tracer
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.

Chemical Information

CAS No. 116815-49-7
Unlabeled CAS 66-99-9
Masse moléculaire 157.17
Formule C₁₀¹³CH₈O
SMILES

O=[13CH]C1=CC2=C(C=CC=C2)C=C1
Livraison

Room temperature in continental US; may vary elsewhere.
Stockage

Please store the product under the recommended conditions in the Certificate of Analysis.

Protocole

All Cell Biology

Cell Viability Determination by MTT Colorimetric Assay
The following protocol uses the MTT colorimetric assay as a classic literature-established method for assessing cell viability/metabolic activity in cultured mammalian cells. MTT[3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] is reduced by metabolically active cells to a colored formazan product; the amount of formazan is quantified spectrophotometrically and provides an indirect measure of metabolically active viable cells. Importantly, MTT reduction reflects cellular oxidoreductase/metabolic activity rather than an absolute direct count of living cells, so changes in cellular metabolism can alter the signal independently of cell number.

Pureté et documentation

Instruction de manipulation (2659 KB)

Références

[1]. Matsushita Y, et al. Antioxidant and cytotoxic activities of naphthalene derivatives from Diospyros kaki. Journal of Wood Science, 2011, 57: 161-165.

[2]. Singh R, et al. Purification and characterization of NAD+ -dependent salicylaldehyde dehydrogenase from carbaryl-degrading Pseudomonas sp. strain C6. Applied biochemistry and biotechnology. 2014 Jan;172(2):806-19. [Content Brief]

[3]. Oladipo SD, et al. Antidiabetes and antioxidant potential of Schiff bases derived from 2-naphthaldehye and substituted aromatic amines: Synthesis, crystal structure, Hirshfeld surface analysis, computational, and studies. Heliyon. 2024 Jan 15;10(1):e23174. [Content Brief]

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How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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Activité biologique
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Chemical Information
Protocole
Pureté et documentation
Références

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2-Naphthaldehyde-13C