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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Oxibendazole - 2mM in DMSO , CAS No.20559-55-1
Disponível para encomenda
GRADE & PURITY 2mM in DMSO
Synonyms
Oxibendazole|20559-55-1|Loditac|Filaribits Plus|Anthelcide EQ|Oxibendazolo|Oxibendazolum|SK&F 30310|Methyl 5-propoxy-2-benzimidazolecarbamate|methyl (5-propoxy-1h-benzo[d]imidazol-2-yl)carbamate|Oxibendazole D7|Oxibendazolum [INN-Latin]|EINECS 243-877-7|O
Shipped In
Dry ice packs + Cold packs
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Why this grade 2mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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 Oxibendazole is a broad-spectrum anthelmintic
Specifications Sinónimos
Oxibendazole | 20559-55-1 | Loditac | Filaribits Plus | Anthelcide EQ | Oxibendazolo | Oxibendazolum | SK&F 30310 | Methyl 5-propoxy-2-benzimidazolecarbamate | methyl (5-propoxy-1h-benzo[d]imidazol-2-yl)carbamate | Oxibendazole D7 | Oxibendazolum [INN-Latin] | EINECS 243-877-7 | O
Especificações e pureza
2mM in DMSO
Mecanismos bioquímicos e fisiológicos
Oxibendazole acts as an anthelmintic heterocyclic compound.Broad spectrum anthelmintic. Binds to β-tubulin and inhibit microtubule formation. Active in vivo . Blood-brain barrier permeable.
Condições de armazenamento de armazenamento
Store at -80°C
Enviado em
Dry ice packs + Cold packs
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Nomes e identificadores Sorrisos canónicos
CCCOC1=CC2=C(C=C1)N=C(N2)NC(=O)OC
IUPAC Name
methyl N-(6-propoxy-1H-benzimidazol-2-yl)carbamate
InChIKey
RAOCRURYZCVHMG-UHFFFAOYSA-N
INCHI
1S/C12H15N3O3/c1-3-6-18-8-4-5-9-10(7-8)14-11(13-9)15-12(16)17-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16)
SMILES isoméricas
CCCOC1=CC2=C(C=C1)N=C(N2)NC(=O)OC
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4193225&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 Classe Benzimidazoles Subclass 2-benzimidazolylcarbamic acid esters Intermediate Tree Nodes Not available Direct Parent 2-benzimidazolylcarbamic acid esters Alternative Parents Alkyl aryl ethers Benzenoids Imidazoles Heteroaromatic compounds Carbamate esters Organic carbonic acids and derivatives Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents 2-benzimidazolylcarbamic acid ester - Alkyl aryl ether - Benzenoid - Azole - Imidazole - Carbamic acid ester - Heteroaromatic compound - Carbonic acid derivative - Ether - Azacycle - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound Descrição This compound belongs to the class of organic compounds known as 2-benzimidazolylcarbamic acid esters. These are aromatic heteropolycyclic compounds that contain a carbamic acid ester group, which is N-linked to the C2-atom of a benzimidazole moiety. 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 Heat Sensitive Ponto de fusão (°C) 216-218°C Peso molecular 249.270 g/mol XLogP3 2.400 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 5 Exact Mass 249.111 Da Monoisotopic Mass 249.111 Da Topological Polar Surface Area 76.200 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 288.000 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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