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1-Naphthol - Ultra pure grade,≥99%, high purity , CAS No.90-15-3

90 Citations COA COA
In stock
Item Number
N128915
Grouped product items
SKU Size
Availability
 Price Qty
N128915-25g
25g
2
$103.90
N128915-50g
50g
1
$165.90
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Metabolite (5307)

Basic Description

Synonyms alpha-Naphthyl alcohol | 1-Naphthol; 1-Naphthalenol; 1-Hydroxynaphthalene; 1-Naphthyl Alcohol; Hydroxynaphthalene | GS-6917 | C.I. Oxidation Base 33 | CI Oxidation Base 33 | N2780_SIAL | Naphthalenol | Z104474036 | 1-Hydroxynaphthalene | 1-Naphthol, Purif
Specifications & Purity Ultra pure, ≥99%
Storage Temp Protected from light
Shipped In Normal
Grade Ultra pure

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Naphthalenes
Subclass Naphthols and derivatives
Intermediate Tree Nodes Not available
Direct Parent Naphthols and derivatives
Alternative Parents 1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Organooxygen compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic homopolycyclic compounds
Substituents 1-naphthol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
Description This compound belongs to the class of organic compounds known as naphthols and derivatives. These are naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position.
External Descriptors a small molecule

Associated Targets(Human)

ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CASP3 Tchem Caspase-3 (3632 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MAPKAPK2 Tchem MAP kinase-activated protein kinase 2 (4814 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A4 Tbio UDP-glucuronosyltransferase 1A4 (288 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2A6 Tchem Cytochrome P450 2A6 (2861 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
K562 (73714 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MOLT-4 (49676 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT2B7 Tchem UDP-glucuronosyltransferase 2B7 (787 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT2B17 Tbio UDP-glucuronosyltransferase 2B17 (197 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT2B4 Tbio UDP-glucuronosyltransferase 2B4 (139 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT2B10 Tbio UDP-glucuronosyltransferase 2B10 (42 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT2B15 Tbio UDP-glucuronosyltransferase 2B15 (172 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT2B28 Tbio UDP-glucuronosyltransferase 2B28 (9 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A1 Tchem UDP-glucuronosyltransferase 1-1 (448 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 (221 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A7 Tbio UDP-glucuronosyltransferase 1-7 (106 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A8 Tbio UDP-glucuronosyltransferase 1-8 (233 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 (343 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT1A10 Tbio UDP-glucuronosyltransferase 1-10 (257 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UGT2A1 UDP-glucuronosyltransferase 2A1 (59 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTGS2 Tclin Cyclooxygenase (1258 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

SULT1E1 Estrogen sulfotransferase (8 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cyp2a5 Cytochrome P450 2A5 (126 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mus musculus (284745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHO (4503 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ced-3 Cell death protein 3 (4 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504751222
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504751222
IUPAC Name naphthalen-1-ol
INCHI InChI=1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H
InChIKey KJCVRFUGPWSIIH-UHFFFAOYSA-N
Smiles C1=CC=C2C(=C1)C=CC=C2O
Isomeric SMILES C1=CC=C2C(=C1)C=CC=C2O
WGK Germany 1
RTECS QL2800000
UN Number 2811
Packing Group III
Molecular Weight 144.17
Beilstein 1817321
Reaxy-Rn 1817321
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1817321&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot Number Certificate Type Date Item
K2429699 Certificate of Analysis Nov 14, 2024 N128915
K2429700 Certificate of Analysis Nov 14, 2024 N128915
H2302727 Certificate of Analysis Jul 10, 2023 N128915
H2302714 Certificate of Analysis Jul 10, 2023 N128915
H2302733 Certificate of Analysis Jul 10, 2023 N128915
H2302731 Certificate of Analysis Jul 10, 2023 N128915
H2421014 Certificate of Analysis Jul 10, 2023 N128915
J2228127 Certificate of Analysis Oct 31, 2022 N128915
G2216428 Certificate of Analysis Jun 30, 2022 N128915
G2216426 Certificate of Analysis Jun 30, 2022 N128915

Chemical and Physical Properties

Sensitivity Air Light Sensitive
Refractive Index 1.6206
Flash Point(°F) 125℃
Flash Point(°C) 125℃
Boil Point(°C) 147°C/15mmHg
Melt Point(°C) 96°C
Molecular Weight 144.170 g/mol
XLogP3 2.800
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 0
Exact Mass 144.058 Da
Monoisotopic Mass 144.058 Da
Topological Polar Surface Area 20.200 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 133.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

How to Cite Aladdin Scientific Products?
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3. Haihong Wang, Huiyan Ma, Yan Li, Lin Cheng, Jucai Yang, Juming Liu.  (2023)  Facile Synthesis of TiO2 with a Narrow Bandgap and Low Valence Band for Efficient Visible-Light Photocatalytic Degradation of Various Phenols.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,  62  (36): (14320–14334). 
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