Iprodione - ≥97% , CAS No.36734-19-7

CAS: 36734-19-7 Cat. No.: D140383 Peso molecular: 330.17 Beilstein Registry Number: 895003 Número EC: 253-178-9
Disponible para pedir
GRADE & PURITY ≥97%
Synonyms
1ST21164 | NCGC00163788-02 | 3-(3,5-DICHLOROPHENYL)-2,4-DIOXO-N-PROPAN-2-YL-IMIDAZOLIDINE-1-CARBOXAMIDE | 3-(3,5-dichlorophenyl)-2,4-dioxo-N-propan-2-ylimidazolidine-1-carboxamide | NCGC00163788-04 | NCGC00163788-05 | Rovral PM | Kidan | UNII-S3AYV2A6EU |
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
D140383-5g
4
104,90US$
25g
D140383-25g
3
381,90US$
100g
D140383-100g
1
1.108,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
1ST21164 | NCGC00163788-02 | 3-(3, 5-DICHLOROPHENYL)-2, 4-DIOXO-N-PROPAN-2-YL-IMIDAZOLIDINE-1-CARBOXAMIDE | 3-(3, 5-dichlorophenyl)-2, 4-dioxo-N-propan-2-ylimidazolidine-1-carboxamide | NCGC00163788-04 | NCGC00163788-05 | Rovral PM | Kidan | UNII-S3AYV2A6EU |
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Tipo de acción
INHIBITOR
Pureza
≥97%
Nombres e identificadores
Pubchem Sid488183290
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488183290
Sonrisas canónicasCC(C)NC(=O)N1CC(=O)N(C1=O)C2=CC(=CC(=C2)Cl)Cl
IUPAC Name3-(3,5-dichlorophenyl)-2,4-dioxo-N-propan-2-ylimidazolidine-1-carboxamide
InChIKeyONUFESLQCSAYKA-UHFFFAOYSA-N
INCHI1S/C13H13Cl2N3O3/c1-7(2)16-12(20)17-6-11(19)18(13(17)21)10-4-8(14)3-9(15)5-10/h3-5,7H,6H2,1-2H3,(H,16,20)
Isómeros SMILES CC(C)NC(=O)N1CC(=O)N(C1=O)C2=CC(=CC(=C2)Cl)Cl
WGK Alemania 3
RTECS NI8870000
Número ONU 3077
Peso molecular 330.17
Beilstein 895003
Reaxy-Rn 895003
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=895003&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
SuperclassOrganoheterocyclic compounds
ClaseAzolidines
SubclassImidazolidines
Intermediate Tree Nodes Imidazolidinones - Imidazolidinediones - Hydantoins
Direct ParentPhenylhydantoins
Alternative Parents Phenylimidazolidines  Alpha amino acids and derivatives  Dichlorobenzenes  N-acyl ureas  Aryl chlorides  Dicarboximides  Isoureas  Propargyl-type 1,3-dipolar organic compounds  Carboximidamides  Azacyclic compounds  Organopnictogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents 3-phenylhydantoin - Phenylimidazolidine - Alpha-amino acid or derivatives - 1,3-dichlorobenzene - Chlorobenzene - Halobenzene - N-acyl urea - Ureide - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Dicarboximide - Urea - Carbonic acid derivative - Isourea - Azacycle - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic 1,3-dipolar compound - Carboximidic acid derivative - Carboxylic acid derivative - Organooxygen compound - Organopnictogen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organohalogen compound - Carbonyl group - Organic nitrogen compound - Organochloride - Organonitrogen compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phenylhydantoins. These are heterocyclic aromatic compounds containing an imiazolidinedione moiety substituted by a phenyl group.
External Descriptors Dicarboximide fungicides
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
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Alternaria solani (773 Activities)
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Trypanosoma cruzi (99888 Activities)
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Botrytis cinerea (4183 Activities)
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L6 (7924 Activities)
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Ceratobasidium cereale (139 Activities)
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Macrophomina phaseolina (474 Activities)
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Rhizoctonia solani (2251 Activities)
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Sclerotinia sclerotiorum (877 Activities)
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Corynespora cassiicola (104 Activities)
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Fulvia fulva (138 Activities)
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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Neofusicoccum australe (78 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pestalotiopsis microspora (57 Activities)
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Diplodia mutila (102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Neofusicoccum luteum (172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas amygdali pv. lachrymans (49 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Monilinia laxa (436 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudoperonospora cubensis (1623 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycogone perniciosa (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ascochyta (23 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

7 results found

Lot NumberCertificate TypeFechaArticulo
C2325302Certificate of AnalysisDec 13, 2024 D140383
C2325296Certificate of AnalysisDec 13, 2024 D140383
C2325288Certificate of AnalysisDec 13, 2024 D140383
C2325290Certificate of AnalysisDec 11, 2024 D140383
C2325294Certificate of AnalysisDec 11, 2024 D140383
C2325295Certificate of AnalysisDec 11, 2024 D140383
L1522168Certificate of AnalysisMay 08, 2023 D140383
Propiedades químicas y físicas
Punto de fusión (°C)136°C
Peso molecular330.160 g/mol
XLogP33.100
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass329.033 Da
Monoisotopic Mass329.033 Da
Topological Polar Surface Area69.700 Ų
Heavy Atom Count21
Formal Charge0
Complexity448.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Yang Li, Xiaohuan Zang, Yahuan Li, Shuaihua Zhang, Chun Wang, Zhi Wang.  (2023)  Selective extraction of fungicides from fruit samples with defective UiO-66 as solid-phase microextraction fiber coating.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2023.108608]
2. Xiaoyu Liang, Yun Peng, Yanchao Liu, Meng Wang, Ye Yang, Yu Zhang.  (2019)  First report of Bipolaris bicolor causing a leaf spot disease on rubber tree.  JOURNAL OF PHYTOPATHOLOGY,  167  (10): (553-557).  [PMID:] [10.1111/jph.12839]
Calculadoras de soluciones
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