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224,000+ productos de investigación · Triple ISO certified · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Pyriproxifen - 10mM in DMSO , CAS No.95737-68-1
GRADE & PURITY 10mM in DMSO
Synonyms
Pyriproxyfen 100 microg/mL in Acetonitrile | JUVENTOX | P2612 | KS-5363 | NCGC00163945-02 | VECTRA FELIS COMPONENT PYRIPROXYFEN | D08455 | Tox21_300716 | UNII-3Q9VOR705O | 2-(1-(4-phenoxyphenoxy)propan-2-yloxy)pyridine | HY-B2031 | NCGC00163945-04 | PYRIP
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
Pyriproxyfen 100 microg/mL in Acetonitrile | JUVENTOX | P2612 | KS-5363 | NCGC00163945-02 | VECTRA FELIS COMPONENT PYRIPROXYFEN | D08455 | Tox21_300716 | UNII-3Q9VOR705O | 2-(1-(4-phenoxyphenoxy)propan-2-yloxy)pyridine | HY-B2031 | NCGC00163945-04 | PYRIP
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Insect juvenile hormone mimetic. Larvicidal agent. Inhibits maturation in a broad spectrum of insect species and sterilizes adult females. Orally active.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas
CC(COC1=CC=C(C=C1)OC2=CC=CC=C2)OC3=CC=CC=N3
IUPAC Name
2-[1-(4-phenoxyphenoxy)propan-2-yloxy]pyridine
InChIKey
NHDHVHZZCFYRSB-UHFFFAOYSA-N
INCHI
1S/C20H19NO3/c1-16(23-20-9-5-6-14-21-20)15-22-17-10-12-19(13-11-17)24-18-7-3-2-4-8-18/h2-14,16H,15H2,1H3
Isómeros SMILES
CC(COC1=CC=C(C=C1)OC2=CC=CC=C2)OC3=CC=CC=N3
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6932868&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 Clase Benzene and substituted derivatives Subclass Diphenylethers Intermediate Tree Nodes Not available Direct Parent Diphenylethers Alternative Parents Diarylethers Phenoxy compounds Phenol ethers Alkyl aryl ethers Pyridines and derivatives Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents Diphenylether - Diaryl ether - Phenoxy compound - Phenol ether - Alkyl aryl ether - Pyridine - Heteroaromatic compound - Ether - Organoheterocyclic compound - Azacycle - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether group. External Descriptors Pesticides 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Punto de fusión (°C) 45-47°C Peso molecular 321.400 g/mol XLogP3 4.800 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 7 Exact Mass 321.136 Da Monoisotopic Mass 321.136 Da Topological Polar Surface Area 40.600 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 338.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 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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