Indoxacarb - analytical standard,Moligand™ , CAS No.144171-61-9

CAS: 144171-61-9 Cat. No.: I133012 Summenformel: C22H17ClF3N3O7 Molekulargewicht: 527.83 EG-Nummer: 604-398-2
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GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.
Synonyms
HY-B0834 | Tox21_303872 | INDOXACARB, (R,S)- | methyl 7-chloro-2-[methoxycarbonyl-[4-(trifluoromethoxy)phenyl]carbamoyl]-3,5-dihydroindeno[1,2-e][1,3,4]oxadiazine-4a-carboxylate | NCGC00357134-01 | DPX-MP 062 | EX-A2190 | INDOXACARB (RS)-FORM [MI] | (+-)-
Storage
Room temperature
Shipped In
Normal
★
Size
Deutschland (EU)
USA*
Price
Qty
5mg
I133012-5mg
Auf Bestellung · 8–12 Wochen
25,95€
25mg
I133012-25mg
Auf Bestellung · 8–12 Wochen
82,35€
100mg
I133012-100mg
Auf Bestellung · 8–12 Wochen
260,23€
250mg
I133012-250mg
—
1 Auf Lager
520,56€
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Why this grade

analytical standard,Moligand™ Analytischer Standard,Moligand™ 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.

📚

Literature proof

Cited in 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Indoxacarb belongs to oxadiazine class of insecticides, showing broad-spectrum activity against Lepidoptera and other pests. Its mode of action involves blocking of voltage-gated sodium channels and binding to neuronal nicotinic acetylcholine receptors. Application Indoxacarb may be used as an analytical reference standard for the quantification of the analyte in foodstuffs of plant and animal origin using gas chromatography with electron capture detection (GC-ECD) and liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS).

Specifications

Synonyme
HY-B0834 | Tox21_303872 | INDOXACARB, (R,S)- | methyl 7-chloro-2-[methoxycarbonyl-[4-(trifluoromethoxy)phenyl]carbamoyl]-3,5-dihydroindeno[1,2-e][1,3,4]oxadiazine-4a-carboxylate | NCGC00357134-01 | DPX-MP 062 | EX-A2190 | INDOXACARB (RS)-FORM [MI] | (+-)-
Spezifikationen & Reinheit
analytical standard,Moligand™
Storage
Room temperature
Verschickt in
Normal
Note
Analytischer Standard, Moligand™
Namen und Kennungen
Pubchem Sid528775406
Kanonisches LächelnCOC(=O)C12CC3=C(C1=NN(CO2)C(=O)N(C4=CC=C(C=C4)OC(F)(F)F)C(=O)OC)C=CC(=C3)Cl
IUPAC Namemethyl 7-chloro-2-[methoxycarbonyl-[4-(trifluoromethoxy)phenyl]carbamoyl]-3,5-dihydroindeno[1,2-e][1,3,4]oxadiazine-4a-carboxylate
InChIKeyVBCVPMMZEGZULK-UHFFFAOYSA-N
INCHI1S/C22H17ClF3N3O7/c1-33-18(30)21-10-12-9-13(23)3-8-16(12)17(21)27-28(11-35-21)19(31)29(20(32)34-2)14-4-6-15(7-5-14)36-22(24,25)26/h3-9H,10-11H2,1-2H3
Isomere SMILES COC(=O)C12CC3=C(C1=NN(CO2)C(=O)N(C4=CC=C(C=C4)OC(F)(F)F)C(=O)OC)C=CC(=C3)Cl
WGK Deutschland 3
Molekulargewicht 527.83
Reaxy-Rn 11322125
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11322125&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

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
KlasseBenzene and substituted derivatives
SubclassPhenylcarbamic acid esters
Intermediate Tree Nodes Not available
Direct ParentPhenylcarbamic acid esters
Alternative Parents N-phenylureas  Indanes  Phenoxy compounds  Phenol ethers  Semicarbazones  Aryl chlorides  Carbamate esters  Methyl esters  Trihalomethanes  Organic carbonic acids and derivatives  Oxacyclic compounds  Azacyclic compounds  Monocarboxylic acids and derivatives  Organofluorides  Hydrocarbon derivatives  Carbonyl compounds  Organopnictogen compounds  Organochlorides  Alkyl fluorides  Organic oxides  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Phenylcarbamic acid ester - N-phenylurea - Indane - Phenoxy compound - Phenol ether - Aryl chloride - Aryl halide - Semicarbazone - Semicarbazide - Carbamic acid ester - Methyl ester - Trihalomethane - Carboxylic acid ester - Carbonic acid derivative - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organofluoride - Organochloride - Organohalogen compound - Alkyl fluoride - Organonitrogen compound - Organic nitrogen compound - Organopnictogen compound - Organooxygen compound - Carbonyl group - Organic oxygen compound - Organic oxide - Alkyl halide - Halomethane - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as phenylcarbamic acid esters. These are ester derivatives of phenylcarbamic acids.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot NumberCertificate TypeDatumArtikel
F2615245Certificate of AnalysisJun 26, 2026 I133012
F2615246Certificate of AnalysisJun 26, 2026 I133012
F2615247Certificate of AnalysisJun 26, 2026 I133012
F2615249Certificate of AnalysisJun 26, 2026 I133012
K2507021Certificate of AnalysisNov 18, 2025 I133012
F23281230Certificate of AnalysisApr 08, 2025 I133012
F23281236Certificate of AnalysisApr 08, 2025 I133012
F23281242Certificate of AnalysisApr 08, 2025 I133012
C2518385Certificate of AnalysisApr 12, 2024 I133012
Chemische und physikalische Eigenschaften
Molekulargewicht527.800 g/mol
XLogP34.800
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count11
Rotatable Bond Count5
Exact Mass527.071 Da
Monoisotopic Mass527.071 Da
Topological Polar Surface Area107.000 Ų
Heavy Atom Count36
Formal Charge0
Complexity912.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referenzen
1. Lei Jiang, Lin Yuan, Shan Gao, Yingying Xiang, Fei Song, Wensi Ma, Jing Wan, Xiuling Ji, Yujiao Tu.  (2023)  Facile hydrothermal synthesis of N-doped fluorescent carbon dots for selective detection of insecticide parathion.  Analytical Methods,  15  (19): (2376-2381).  [PMID:37132329] [10.1039/D3AY00124E]
2. Yifan Li, Shujun Ni, Yunping Wang, Ruichi Li, Hong Sun, Xuan Ye, Zhen Tian, Yalin Zhang, Jiyuan Liu.  (2023)  The chemosensory protein 1 contributes to indoxacarb resistance in Plutella xylostella (L.).  PEST MANAGEMENT SCIENCE,      [PMID:36809665] [10.1002/ps.7415]
3. Jun Zhang, Fei Xue, Zhonggang Wang.  (2022)  AIE-Active Fluorescent Porous Polymers for Recognizable Detection of Imidacloprid and Structure–Property Relationship.  CHEMISTRY OF MATERIALS,      [PMID:] [10.1021/acs.chemmater.2c02867]
4. Yujie Zhang, Yunlong Huang, Ling Fu, Jiaoyan Qiu, Zhuqing Wang, Aiguo Wu.  (2020)  Colorimetric detection of paraquat in aqueous and fruit juice samples based on functionalized gold nanoparticles.  JOURNAL OF FOOD COMPOSITION AND ANALYSIS,      [PMID:] [10.1016/j.jfca.2020.103574]
5. Jing-yan Kang, Yu-jie Zhang, Xing Li, Chen Dong, Hong-yu Liu, Li-jing Miao, Paul J. Low, Zhi-xian Gao, Narayan S. Hosmane, Ai-guo Wu.  (2017)  Rapid and sensitive colorimetric sensing of the insecticide pymetrozine using melamine-modified gold nanoparticles.  Analytical Methods,  10  (4): (417-421).  [PMID:] [10.1039/C7AY02658G]
6. Weiqian Liang, Juntao Wang, Xiaohuan Zang, Wenhuan Dong, Chun Wang, Zhi Wang.  (2017)  Barley husk carbon as the fiber coating for the solid-phase microextraction of twelve pesticides in vegetables prior to gas chromatography–mass spectrometric detection.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:28237260] [10.1016/j.chroma.2017.02.034]
7. Xinyue Huang, Lei Jiang, Lin Yuan, Wensi Ma, Xintao Cui, Jiaxuan Liu, Xiuling Ji, YujiaoTu.  (2025)  Orange ratiometric fluorescent probe for sensitive detection of phoxim.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:40795714] [10.1016/j.saa.2025.126785]
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