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1-Naphthalenemethanol

1-Naphthalenemethanol is a hydroxyl-substituted naphthalene derivative. 1-Naphthalenemethanol can be extracted from the root of Annona senegalensis. 1-Naphthalenemethanol is a photolysis product of 1-napthaleneacetic acid. 1-Naphthalenemethanol, together with PAPS, provides some protection against the irreversible inactivation of AST IV caused by N-OH-2AF. 1-Naphthalenemethanol can be used in antibacterial research[1][2][3][4].

Product Specifications

CAS Number

[4780-79-4]

Product Name Alternative

1-Hydroxymethylnaphthalene

UNSPSC

12352005

Hazard Statement

H302, H315, H319, H335

Target

Bacterial; Biochemical Assay Reagents

Type

Natural Products

Related Pathways

Anti-infection; Others

Applications

COVID-19-immunoregulation

Field of Research

Infection

Assay Protocol

https://www.medchemexpress.com/1-naphthalenemethanol.html

Concentration

10mM

Purity

99.97

Solubility

DMSO : 100 mg/mL (ultrasonic)

Smiles

OCC1=C2C=CC=CC2=CC=C1

Molecular Formula

C11H10O

Molecular Weight

158.20

Precautions

H302, H315, H319, H335

References & Citations

[1]Theophine Chinwuba Okoye, et al. Antimicrobial Effects of a Lipophilic Fraction and Kaurenoic Acid Isolated from the Root Bark Extracts of Annona senegalensis. Evid Based Complement Alternat Med. 2012;2012:831327.|[2]Feng Y L, et al. UV light induced transformation of 1-methylnaphthalene in the presence of air and its implications for contaminants research. 2012.|[3]King RS, et al. Oxidation-dependent inactivation of aryl sulfotransferase IV by primary N-hydroxy arylamines during in vitro assays. Carcinogenesis. 1997 Apr;18 (4) :843-9.|[4]Crosby D G, et al. Photodecomposition of 1-naphthaleneacetic acid[J]. Journal of Agricultural and Food Chemistry, 1969, 17 (6) : 1291-1293.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Natural Products

Clinical Information

No Development Reported

Available Sizes

Curated Selection

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