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N1000

Sigma-Aldrich

1-Naphthol

ReagentPlus®, ≥99%

Synonyme(s) :

1-hydroxynaphthalène, α-naphthol

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About This Item

Formule linéaire :
C10H7OH
Numéro CAS:
Poids moléculaire :
144.17
Numéro Beilstein :
1817321
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.21

Densité de vapeur

4.5 (120 °C, vs air)

Niveau de qualité

Pression de vapeur

1 mmHg ( 94 °C)

Gamme de produits

ReagentPlus®

Pureté

≥99%

Température d'inflammation spontanée

1007 °F

Limite d'explosivité

5 %

Couleur

white to off-white

Point d'ébullition

278-280 °C (lit.)

Pf

94-96 °C (lit.)

Fluorescence

λex 300 nm; λem 472 nm (Borax buffer)

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Chaîne SMILES 

Oc1cccc2ccccc12

InChI

1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H

Clé InChI

KJCVRFUGPWSIIH-UHFFFAOYSA-N

Informations sur le gène

human ... CYP1A2(1544)

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Description générale

1-Naphthol is a hydroxyl-aromatic compound. Its thermodynamic properties such as heat capacity, sublimation pressure, vapor pressure, enthalpies of combustion, formation and fusion have been estimated. The decomposition of 1-naphthol in aqueous solutions on exposure to gamma radiation has been studied. The ability of biochar of orange peels in adsorbing 1-naphthol from water has been investigated. The activation energy and the reaction rate constant of the enzymatic polymerization of 1-naphthol using laccase have been reported. It undergoes hydrogenation in the presence of a rhodium catalyst to form cis,cis 1-decalol. This product is a certified reference material (CRM) certified to International Standards BS EN ISO / IEC 17025 and ISO 17034 under UKAS accreditation.

Application

1-Naphthol has been used as a prooxidant to analyze its ability to induce hemolysis in a zebrafish G6PD (glucose-6-phosphate dehydrogenase) deficiency model.

Informations légales

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1A - STOT SE 2 Oral - STOT SE 3

Organes cibles

Kidney, Respiratory system

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

257.0 °F - closed cup

Point d'éclair (°C)

125 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Les clients ont également consulté

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Thermodynamic properties of 1-naphthol: Mutual validation of experimental and computational results.
Chirico RD, et al.
The Journal of Chemical Thermodynamics, 86, 106-115 (2015)
Reaction kinetics for laccase-catalyzed polymerization of 1-naphthol.
Aktas N, et al.
Bioresource Technology, 80(1), 29-36 (2001)
Xiaobai Patrinostro et al.
Experimental hematology, 41(8), 697-710 (2013-04-23)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common genetic defect and enzymopathy worldwide, affecting approximately 400 million people and causing acute hemolysis in persons exposed to prooxidant compounds such as menthol, naphthalene, antimalarial drugs, and fava beans. Mouse models have
Hydrogenation of 1-naphthol with rhodium catalyst.
Freifelder M and Stone GR.
Journal of Pharmaceutical Sciences, 53(9), 1134-1135 (1964)
Radiolysis of 1-naphthol in aqueous solutions.
Ngo TM, et al.
J. Radioanal. Nucl. Chem., 286(1), 287-293 (2010)

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