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· · COA & SDS available for every product · Same-day shipping on in-stock items 5-Hydroxyindole - Moligand™, ≥98% , Allosteric modulator of 5-HT 3A, CAS No.1953-54-4, Allosteric modulator of 5-HT 3A
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98% Synonyms
5-hydroxy indole | AC-5464 | DTXSID00173187 | EN300-79057 | Hydroxy-5 indole [French] | SCHEMBL50566 | H-6044 | AKOS005206937 | 1h-indole-5-ol | 1H-indol-5-ol. | 3fuh | UNII-320UN7XZYN | (R)-(+)-7-Methoxy2-aminotetralin | 5-21-03-00018 (Beilstein Handboo
Storage
Store at 2-8°C,Protected from light,Argon charged
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Why this grade Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light,Argon charged Ships Wet ice 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 Reactants for the preparation of antitumor agents (oximidazolyl / oxpyrimidinyl) benzenesulfonate and tubulin inhibitors
Reactants for preparation of o-aminobenzoic acid
It is used to prepare indole compounds as reactants of dopamine D2 receptor antagonists
Reactants for preparation of human β - adrenoceptor ligands containing naphthalimide or carbazole
Reactants for preparation of natural radiation protective agent melanin
Reactants for the preparation of 5-vinyl-3-pyridinonitrile, a PKC θ inhibitor
Specifications Synonyms
5-hydroxy indole | AC-5464 | DTXSID00173187 | EN300-79057 | Hydroxy-5 indole [French] | SCHEMBL50566 | H-6044 | AKOS005206937 | 1h-indole-5-ol | 1H-indol-5-ol. | 3fuh | UNII-320UN7XZYN | (R)-(+)-7-Methoxy2-aminotetralin | 5-21-03-00018 (Beilstein Handboo
Specifications & Purity
Moligand™, ≥98%
Storage
Store at 2-8°C, Protected from light, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
ALLOSTERIC MODULATOR
Mechanism of action
Allosteric modulator of 5-HT 3A
Names and Identifiers Pubchem Sid 504752730 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504752730 Canonical Smiles C1=CC2=C(C=CN2)C=C1O IUPAC Name 1H-indol-5-ol InChIKey LMIQERWZRIFWNZ-UHFFFAOYSA-N INCHI 1S/C8H7NO/c10-7-1-2-8-6(5-7)3-4-9-8/h1-5,9-10H Isomeric SMILES C1=CC2=C(C=CN2)C=C1O WGK Germany 3 RTECS NM2430000 Molecular Weight 133.15 Beilstein 112349 Reaxy-Rn 112349 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=112349&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 Organoheterocyclic compounds Class Indoles and derivatives Subclass Hydroxyindoles Intermediate Tree Nodes Not available Direct Parent Hydroxyindoles Alternative Parents Indoles 1-hydroxy-2-unsubstituted benzenoids Pyrroles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Hydroxyindole - Indole - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as hydroxyindoles. These are organic compounds containing an indole moiety that carries a hydroxyl group. External Descriptors Not available 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 Sensitivity Air sensitive ，Light sensitive Melt Point(°C) 107-110°C Molecular Weight 133.150 g/mol XLogP3 2.000 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 0 Exact Mass 133.053 Da Monoisotopic Mass 133.053 Da Topological Polar Surface Area 36.000 Ų Heavy Atom Count 10 Formal Charge 0 Complexity 126.000 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
Documents & Articles Solution Calculators Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Reviews Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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