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Mandipropamid

Mandipropamid Suppliers list
Company Name: Hubei Zhengxingyuan Fine Chemical Co., Ltd.  
Tel: 027-027-87879189 15207106154
Email: 3386829764@qq.com
Company Name: Manhag Testing Technology Co., Ltd  
Tel: 400-818 0104 18918165978
Email: yanyan.guo@bestown.net.cn
Mandipropamid Basic information
Product Name:Mandipropamid
Synonyms:Mandipropamid;noa 446510;2-(4-Chlorophenyl)-N-[2-[3-methoxy-4-(prop-2-ynyloxy)phenyl]ethyl]-2-(prop-2-ynyloxy)acetamide;2-(4-Chlorophenyl)-N-[3-methoxy-4-(2-propynyloxy)phenethyl]-2-(2-propynyloxy)acetamide;Mandipropamid [iso];2-(4-chlorophenyl)-N-(2-Methoxy-4-(prop-2-yn-1-yloxy)phenethyl)-2-(prop-2-yn-1-yloxy)acetaMide;Mandipropamid Standard;Mandipropamid Solution, 1000ppm
CAS:374726-62-2
MF:C23H22ClNO4
MW:411.88
EINECS:
Product Categories:
Mol File:374726-62-2.mol
Mandipropamid Structure
Mandipropamid Chemical Properties
Melting point 96-97 °C
Boiling point 608.6±55.0 °C(Predicted)
density 1.214±0.06 g/cm3(Predicted)
storage temp. Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility Chloroform (Slightly), Dichloromethane (Slightly)
form powder
pka13.90±0.46(Predicted)
color Pale Beige
Henry's Law Constant1.1×104 mol/(m3Pa) at 25℃, HSDB (2015)
Major Applicationagriculture
environmental
InChI1S/C23H22ClNO4/c1-4-14-28-20-11-6-17(16-21(20)27-3)12-13-25-23(26)22(29-15-5-2)18-7-9-19(24)10-8-18/h1-2,6-11,16,22H,12-15H2,3H3,(H,25,26)
InChIKeyKWLVWJPJKJMCSH-UHFFFAOYSA-N
SMILESClC1=CC=C(C(OCC#C)C(NCCC2=CC=C(OCC#C)C(OC)=C2)=O)C=C1
LogP4.160 (est)
EPA Substance Registry SystemBenzeneacetamide, 4-chloro-N-[2-[3-methoxy-4-(2-propyn-1-yloxy)phenyl]ethyl]-.alpha.-(2-propyn-1-yloxy)- (374726-62-2)
Safety Information
WGK Germany 3
Storage Class11 - Combustible Solids
Hazard ClassificationsAquatic Acute 1
Aquatic Chronic 1
Hazardous Substances Data374726-62-2(Hazardous Substances Data)
MSDS Information
Mandipropamid Usage And Synthesis
Chemical PropertiesDicynamid pure product is light yellow powder, melting point 96.4~97.3 ℃, vapor pressure <9.4×10-4mPa(25~50 ℃), distribution coefficient Kow lgP=3.2, Henry's coefficient <9.2×10-5 Pa-m3/mol(25 ℃, calculated value), density(22 ℃)1.24g/L. Solubility in water 4.2mg Solubility in water 4.2mg/L(25℃); Solubility in organic solvents (25℃, g/L): n-hexane 0.042, n-octanol 4.8, toluene 29, methanol 66, ethyl acetate 120, acetone 300, dichloromethane 400 Stable in pH=4~9.
UsesMandipropamid is a fungicide. It can be used on many fruit and vegetable crops, including potatoes, tomatoes, salad leaves and grapes. Manufactured by Syngenta.
DefinitionChEBI: 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide is a monocarboxylic acid amide resulting from the condensation of the carboxy group of p-chloromandelic acid propargyl ether with the amino group of 2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethylamine. It is a monocarboxylic acid amide, a terminal acetylenic compound, an aromatic ether and a member of monochlorobenzenes.
Production MethodsThe industrial production of mandipropamid begins with the preparation of key intermediates such as 4-chloroacetophenone and vanillin, which undergo condensation and oxidation reactions to form a substituted aromatic ketone. This intermediate is then coupled with a cyclopropyl-containing oxazole derivative through a Friedel–Crafts acylation or similar electrophilic substitution, forming the central methanone bridge. The next step involves constructing the amide bond by reacting the ketone with an amine or ammonia derivative under mild conditions, yielding the final active compound: (RS)-2-(4-chlorophenyl)-N-(cyclopropylmethoxy)-N-(2-methoxyphenyl)acetamide. The synthesis is optimised to avoid protecting groups, simplifying purification and reducing waste.
Biological ActivityMandipropamid (Mandi) is an agrochemical extensively used as fungicide. Mandipropamid specifically induces complex formation between a sixfold mutant of the plant hormone receptor pyrabactin resistance 1 (PYR1) and abscisic acid insensitive (ABI). Mandipropamid is a highly cell permeable, low toxic chemical inducers of proximity in vivo. It induces rapid colocalization of proteins contained fused receptor domain PYRMandi and receiver domain ABI.
Mechanism of actionInhibits spore germination with preventative action. Cellulose synthesis inhibitor.
storageStore at -20°C
Pesticide TypeFungicide
Tag:Mandipropamid(374726-62-2) Related Product Information
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