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· · COA & SDS available for every product · Same-day shipping on in-stock items Butenafine HCl - ≥98%(HPLC) , Squalene monooxygenase inhibitor, CAS No.101827-46-7, Squalene monooxygenase inhibitor
Synonyms
FT-0699734 | MLS003899213 | N-[4-(tert-Butyl)benzyl]-N-methyl-1-(1-naphthyl)methanamine Hydrochloride | 1-(4-tert-butylphenyl)-N-methyl-N-(naphthalen-1-ylmethyl)methanamine hydrochloride | SCHEMBL262301 | N-((4-(1,1-Dimethylethyl)phenyl)methyl)-N-methyl-1
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Why this grade ≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview A compound with antifungal properties
Specifications Synonyms
FT-0699734 | MLS003899213 | N-[4-(tert-Butyl)benzyl]-N-methyl-1-(1-naphthyl)methanamine Hydrochloride | 1-(4-tert-butylphenyl)-N-methyl-N-(naphthalen-1-ylmethyl)methanamine hydrochloride | SCHEMBL262301 | N-((4-(1, 1-Dimethylethyl)phenyl)methyl)-N-methyl-1
Specifications & Purity
≥98%(HPLC)
Biochemical and Physiological Mechanisms
Butenafine Hydrochloride has antifungal properties and inhibits sterol synthesis by inhibiting squalene epoxidase.
Mechanism of action
Squalene monooxygenase inhibitor
Names and Identifiers Pubchem Sid 488189816 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488189816 Canonical Smiles CC(C)(C)C1=CC=C(C=C1)CN(C)CC2=CC=CC3=CC=CC=C32.Cl IUPAC Name 1-(4-tert-butylphenyl)-N-methyl-N-(naphthalen-1-ylmethyl)methanamine;hydrochloride InChIKey LJBSAUIFGPSHCN-UHFFFAOYSA-N INCHI 1S/C23H27N.ClH/c1-23(2,3)21-14-12-18(13-15-21)16-24(4)17-20-10-7-9-19-8-5-6-11-22(19)20;/h5-15H,16-17H2,1-4H3;1H Isomeric SMILES CC(C)(C)C1=CC=C(C=C1)CN(C)CC2=CC=CC3=CC=CC=C32.Cl RTECS QJ8585000 Alternate CAS 101827-46-7 MeSH Entry Terms butenafine;butenafine HCl;butenafine hydrochloride;KP 363;KP-363;Mentax;N-(p-tert-butylbenzyl)-N-methyl-1-naphthalenemethylamine;N-4-tert-butylbenzyl-N-methyl-1-naphthalene methylamine hydrochloride Molecular Weight 353.93 Reaxy-Rn 11343366 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11343366&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Class Naphthalenes Subclass Not available Intermediate Tree Nodes Not available Direct Parent Naphthalenes Alternative Parents Phenylpropanes Phenylmethylamines Benzylamines Aralkylamines Trialkylamines Organopnictogen compounds Hydrochlorides Hydrocarbon derivatives Molecular Framework Aromatic homopolycyclic compounds Substituents Naphthalene - Phenylpropane - Phenylmethylamine - Benzylamine - Aralkylamine - Monocyclic benzene moiety - Tertiary aliphatic amine - Tertiary amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Organonitrogen compound - Amine - Aromatic homopolycyclic compound Description This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings. External Descriptors ammonium salt - hydrochloride Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility DMSO 70 mg/mL (197.77 mM);Ethanol 70 mg/mL (197.77 mM);Water <1 mg/mL (<1 mM) Melt Point(°C) 208-210°C Molecular Weight 353.900 g/mol XLogP3 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 5 Exact Mass 353.191 Da Monoisotopic Mass 353.191 Da Topological Polar Surface Area 3.200 Ų Heavy Atom Count 25 Formal Charge 0 Complexity 374.000 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 2
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