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Propanil solution - analytical standard,0.100mg/ml in methanol, high purity , CAS No.709-98-8

In stock
Item Number
P114539
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Price Qty
P114539-1ml
1ml
1
$62.90

Basic Description

Synonyms propanil | 709-98-8 | N-(3,4-Dichlorophenyl)propanamide | Propanide | Propanex | Dipram | Grascide | Propanid | Stampede | Supernox | Surcopur | Rogue | Chem Rice | STAM | Synpran N | Cekupropanil | Riselect | Herbax | Strel | Propanamide, N-(3,4-dichlorophenyl)- | Prop job | Montrose propanil | 3'
Specifications & Purity analytical standard, 0.100mg/ml in methanol
Storage Temp Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade analytical standard

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Anilides
Intermediate Tree Nodes Not available
Direct Parent Anilides
Alternative Parents N-arylamides  Dichlorobenzenes  Aryl chlorides  Secondary carboxylic acid amides  Organopnictogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aromatic 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
Description This 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

Associated Targets(Human)

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Echinochloa crus-galli (3685 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Oryza sativa (2923 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Triticum aestivum (1582 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trichomonas vaginalis (2376 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
FTL Ferritin light chain (43324 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name N-(3,4-dichlorophenyl)propanamide
INCHI InChI=1S/C9H9Cl2NO/c1-2-9(13)12-6-3-4-7(10)8(11)5-6/h3-5H,2H2,1H3,(H,12,13)
InChIKey LFULEKSKNZEWOE-UHFFFAOYSA-N
Smiles CCC(=O)NC1=CC(=C(C=C1)Cl)Cl
Isomeric SMILES CCC(=O)NC1=CC(=C(C=C1)Cl)Cl
WGK Germany 3
RTECS UE4900000
UN Number 3077
Packing Group III
Molecular Weight 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=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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 Number Certificate Type Date Item
J1527059 Certificate of Analysis May 10, 2023 P114539

Chemical and Physical Properties

Sensitivity Light sensitive.
Flash Point(°C) >100°C
Molecular Weight 218.080 g/mol
XLogP3 3.100
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 2
Exact Mass 217.006 Da
Monoisotopic Mass 217.006 Da
Topological Polar Surface Area 29.100 Ų
Heavy Atom Count 13
Formal Charge 0
Complexity 186.000
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

Citations of This Product

1. Haoyun Hu, Wenjuan Feng, Rui Shi, Hong Pan, Cheng Liu, Guihua Ruan, Yipeng Huang.  (2024)  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,  1713  (464497). 
2. Yi Wu, Liyuan Zhang, Dongjie Zhang, Runzhong Yu.  (2024)  A surface molecularly imprinted microfluidic paper based device with smartphone assisted colorimetric detection for butachlor in mung bean.  FOOD CHEMISTRY,  435  (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). 
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). 
5. Xiaoou Wei, Yue Sun, Chao Liu, Zhihua Li, Xiaobo Zou, Di Zhang, Wen Zhang, Jiyong Shi, Xiaowei Huang, Yanxiao Li.  (2021)  A nitrile-mediated SERS aptasensor coupled with magnetic separation for optical interference-free detection of atrazine.  SENSORS AND ACTUATORS B-CHEMICAL,  329  (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). 
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,  199  (110259). 

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