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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Thiambutosine - Moligand™, ≥95% , CAS No.500-89-0
Disponível para encomenda
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. ≥95% Synonyms
Thiambutosine | Thiambutosin | Ciba 1906 | Summit 1906 | SU 1906 | NSC 682 | 1-(p-Butoxyphenyl)-3-(p-dimethylaminophenyl)-2-thiourea | CIBA-1906 | NSC-682 | 4-Butoxy-4'-(dimethylamino)thiocarbanilide | CARBANILIDE, 4-BUTOXY-4'-(DIMETHYLAMINO)THIO- | X92J9
Storage
Store at 2-8°C,Protected from light
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Why this grade Moligand™, ≥95% 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 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.
Visão geral
Thiambutosine is an inhibitor of Mycobacterium leprae. In animal experiments, Thiambutosine can inhibit leprosy infection by intramuscular injection.
Specifications Sinónimos
Thiambutosine | Thiambutosin | Ciba 1906 | Summit 1906 | SU 1906 | NSC 682 | 1-(p-Butoxyphenyl)-3-(p-dimethylaminophenyl)-2-thiourea | CIBA-1906 | NSC-682 | 4-Butoxy-4'-(dimethylamino)thiocarbanilide | CARBANILIDE, 4-BUTOXY-4'-(DIMETHYLAMINO)THIO- | X92J9
Especificações e pureza
Moligand™, ≥95%
Condições de armazenamento de armazenamento
Store at 2-8°C,Protected from light
Enviado em
Wet ice
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Propriedades do produto Nomes e identificadores Sorrisos canónicos
CCCCOC1=CC=C(C=C1)NC(=S)NC2=CC=C(C=C2)N(C)C
IUPAC Name
1-(4-butoxyphenyl)-3-[4-(dimethylamino)phenyl]thiourea
InChIKey
JYCBKPOKWDDOOV-UHFFFAOYSA-N
INCHI
1S/C19H25N3OS/c1-4-5-14-23-18-12-8-16(9-13-18)21-19(24)20-15-6-10-17(11-7-15)22(2)3/h6-13H,4-5,14H2,1-3H3,(H2,20,21,24)
SMILES isoméricas
CCCCOC1=CC=C(C=C1)NC(=S)NC2=CC=C(C=C2)N(C)C
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 Classe Benzene and substituted derivatives Subclass N-phenylthioureas Intermediate Tree Nodes Not available Direct Parent N-phenylthioureas Alternative Parents Phenoxy compounds Phenol ethers Dialkylarylamines Aniline and substituted anilines Alkyl aryl ethers Thioureas Organopnictogen compounds Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents N-phenylthiourea - Phenol ether - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Phenoxy compound - Alkyl aryl ether - Thiourea - Tertiary amine - Ether - Amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound Descrição This compound belongs to the class of organic compounds known as n-phenylthioureas. These are compounds containing a N-phenylthiourea moiety, which is structurally characterized by a phenyl group linked to one nitrogen atom of a thiourea 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.
Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Sensibilidade Light sensitive Peso molecular 343.500 g/mol XLogP3 4.400 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 7 Exact Mass 343.172 Da Monoisotopic Mass 343.172 Da Topological Polar Surface Area 68.600 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 362.000 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
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Reconstitution Calculator Revisões 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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