Solución de propanilo - patrón analítico, 100μg/ml en etanol , CAS No.709-98-8

CAS: 709-98-8 Cat. No.: P114541 Peso molecular: 218.08 Beilstein Registry Number: 2365645 Número EC: 211-914-6
Disponible para pedir
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. 100μg/ml in ethanol
Synonyms
Herbax 3E | Montrose propanil | NSC-31312 | Grascide | MLS002207241 | PROPANIL [HSDB] | Vertac Propanil 4 | Surcopur | 3',4'-Dichlorophenylpropionanilide | Cekupropanil | Dichloropropionanilide | Herbax técnica | Propionanilide,4'-dichloro- | Rogue | 3.-P
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
P114541-1ml
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
28,90US$
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Why this grade

patrón analítico, 100μg/ml en etanol Analytical standard 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.

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Literature proof

Cited in 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
Herbax 3E | Montrose propanil | NSC-31312 | Grascide | MLS002207241 | PROPANIL [HSDB] | Vertac Propanil 4 | Surcopur | 3', 4'-Dichlorophenylpropionanilide | Cekupropanil | Dichloropropionanilide | Herbax técnica | Propionanilide, 4'-dichloro- | Rogue | 3.-P
Especificaciones y pureza
patrón analítico, 100μg/ml en etanol
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
Analytical standard
Nombres e identificadores
Sonrisas canónicasCCC(=O)NC1=CC(=C(C=C1)Cl)Cl
IUPAC NameN-(3,4-dichlorophenyl)propanamide
InChIKeyLFULEKSKNZEWOE-UHFFFAOYSA-N
INCHI1S/C9H9Cl2NO/c1-2-9(13)12-6-3-4-7(10)8(11)5-6/h3-5H,2H2,1H3,(H,12,13)
Isómeros SMILES CCC(=O)NC1=CC(=C(C=C1)Cl)Cl
WGK Alemania 3
RTECS UE4900000
Número ONU 3077
Grupo de embalaje III
Peso molecular 218.08
Beilstein 2365645
Reaxy-Rn 2365645
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2365645&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
ClaseBenzene and substituted derivatives
SubclassAnilides
Intermediate Tree Nodes Not available
Direct ParentAnilides
Alternative Parents N-arylamides  Dichlorobenzenes  Aryl chlorides  Secondary carboxylic acid amides  Organopnictogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Anilide - 1,2-dichlorobenzene - N-arylamide - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Organochloride - Organohalogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution.
External Descriptors Anilide herbicides
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Echinochloa crus-galli (3685 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Oryza sativa (2923 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Triticum aestivum (1582 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trichomonas vaginalis (2376 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
FTL Ferritin light chain (43324 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.

1 results found

Lot NumberCertificate TypeFechaArticulo
I1524109Certificate of AnalysisMar 16, 2023 P114541
Propiedades químicas y físicas
SensibilidadLight sensitive.
Punto de inflamación (°C)>100°C
Peso molecular218.080 g/mol
XLogP33.100
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count2
Exact Mass217.006 Da
Monoisotopic Mass217.006 Da
Topological Polar Surface Area29.100 Ų
Heavy Atom Count13
Formal Charge0
Complexity186.000
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. Haoyun Hu, Wenjuan Feng, Rui Shi, Hong Pan, Cheng Liu, Guihua Ruan, Yipeng Huang.  (2023)  Magnetic porous carbon material derived from imine-linked covalent organic frameworks for magnetic solid phase extraction of trace chlorine-containing herbicides in soil.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:37976904] [10.1016/j.chroma.2023.464497]
2. Yi Wu, Liyuan Zhang, Dongjie Zhang, Runzhong Yu.  (2023)  A surface molecularly imprinted microfluidic paper based device with smartphone assisted colorimetric detection for butachlor in mung bean.  FOOD CHEMISTRY,      [PMID:37816277] [10.1016/j.foodchem.2023.137659]
3. Yuhang Wan, Xinyu Yuan, Jia Liu, Ding Zhang, Zhengyong Zhang, Min Sha.  (2023)  Efficient determination of pesticides in rice by QuEChERS and UV spectroscopy in combination with chemometrics.  CEREAL CHEMISTRY,  100  (5): (1106-1113).  [PMID:] [10.1002/cche.10692]
4. Hong Pan, Zushan Gan, Haoyun Hu, Cheng Liu, Yipeng Huang, Guihua Ruan.  (2022)  Magnetic phenolic resin core-shell structure derived carbon microspheres for ultrafast magnetic solid-phase extraction of triazine herbicides.  JOURNAL OF SEPARATION SCIENCE,  45  (14): (2687-2698).  [PMID:35579607] [10.1002/jssc.202200283]
5. Xiaoou Wei, Yue Sun, Chao Liu, Zhihua Li, Xiaobo Zou, Di Zhang, Wen Zhang, Jiyong Shi, Xiaowei Huang, Yanxiao Li.  (2020)  A nitrile-mediated SERS aptasensor coupled with magnetic separation for optical interference-free detection of atrazine.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2020.129075]
6. Xia Guangping, Hu Haoyun, Huang Yipeng, Ruan Guihua.  (2024)  Controllable synthesis of uniform flower-shaped covalent organic framework microspheres as absorbent for solid-phase extraction of trace 2,4-dichlorophenol.  MICROCHIMICA ACTA,  191  (2): (1-10).  [PMID:38216807] [10.1007/s00604-024-06178-7]
7. Guangping Xia, Yipeng Huang, Shi Yu, Bingmei Lai, Zhenyu Li, Guihua Ruan.  (2024)  Facile synthesis of uniform, spherical, nitrogen- and sulfur-rich covalent organic frameworks for efficient extraction of herbicides containing chlorophenyl and acylamino groups.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.110259]
8. Rui Shi, Yipeng Huang, Guihua Ruan, Zhengyi Chen, Yanqun Yang, Zhuqiang Wu.  (2024)  Controlled synthesis of sulfhydryl-dendritic mesoporous silica nanospheres for ultrafast extraction and sensitive analysis of organochlorine herbicides containing amide groups.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:38484640] [10.1016/j.chroma.2024.464794]
9. Yingying Qian, Houyu Yu, Qihuan He, Dandan Fan, Gerben J. Zylstra, Hancheng Wang, Xing Huang.  (2025)  A Novel Trifunctional Hydrolase Cleaving C−O, C−N, and C−C Bonds and Its Widespread Distribution in Proteobacteria and Actinobacteria.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:40555018] [10.1016/j.jhazmat.2025.139002]
10. Yang Bingnian, Peng Ziqin, Xia Guangping, Ruan Guihua, Huang Yipeng, Tang Ningli.  (2026)  Controllable synthesis of reticulated covalent organic polymers for the rapid extraction of triazine herbicides in vegetables prior to analysis by high-performance liquid chromatography.  MICROCHIMICA ACTA,  193  (3): (150).  [PMID:41663847] [10.1007/s00604-026-07841-x]
11. Xiaowen Huang, Zhuqiang Wu, Yipeng Huang, Guihua Ruan, Ningli Tang.  (2026)  Controllable Synthesis of Hydrangea-Shaped Covalent Organic Frameworks by Solvent Tuning at Room Temperature for Solid-Phase Extraction of Herbicides.  LANGMUIR,      [PMID:41563044] [10.1021/acs.langmuir.5c04930]
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