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Orysastrobin

Orysastrobin Suppliers list
Company Name: Qingdao Trust Agri Chemical Co.,Ltd
Tel: +86-008615963231493 +86-008613573296305
Email: trustagri@hotmail.com
Products Intro: Product Name:orysastrobin
CAS:248593-16-0
Purity:99 Package:25kg
Company Name: Hefei TNJ Chemical Industry Co.,Ltd.
Tel: +86-0551-65418684 +86-18949823763
Email: sales@tnjchem.com
Products Intro: Product Name:Orysastrobin
CAS:248593-16-0
Company Name: TargetMol Chemicals Inc.
Tel: 13564774135
Email: marketing@targetmol.com
Products Intro: Product Name:Orysastrobin
CAS:248593-16-0
Package:25mg;|100mg;|50mg;
Company Name: DAYANG CHEM (HANGZHOU) CO.,LTD
Tel: +86-88938639 +86-17705817739
Email: info@dycnchem.com
Products Intro: Product Name:Orysastrobin
CAS:248593-16-0
Purity:0.95&0.99 Package:0.1KG;1KG;1000KG Remarks:High quality
Company Name: Shanghai Kewel Chemical Co., Ltd.  
Tel: 021-64609169 18901607656
Email: greensnown@163.com
Products Intro: Product Name:Orysastrobin
CAS:248593-16-0
Purity:95+ HPLC; Package:10mg;25mg;50mg;100mg

Orysastrobin manufacturers

  • Orysastrobin
  • Orysastrobin pictures
  • 2026-07-15
  • CAS:248593-16-0
  • Purity:
  • Supply Ability: 10g
  • orysastrobin
  • orysastrobin	 pictures
  • 2026-07-14
  • CAS:248593-16-0
  • Min. Order: 1kg
  • Purity: 99
  • Supply Ability: 20tons
Orysastrobin Basic information
Product Name:Orysastrobin
Synonyms:Orysastrobin;bas520f;ORYSASTROBIN STANDARD;Orysastrobin [iso];Orysastrobin Solution, 100ppm;Benzeneacetamide, α-(methoxyimino)-2-[(3E,5E,6E)-5-(methoxyimino)-4,6-dimethyl-2,8-dioxa-3,7-diazanona-3,6-dien-1-yl]-N-methyl-, (αE)-;C15749000 Orysastrobin;XA15749000ALOrysastrobin 100μg/mLin Acetonitr
CAS:248593-16-0
MF:C18H25N5O5
MW:391.43
EINECS:
Product Categories:
Mol File:248593-16-0.mol
Orysastrobin Structure
Orysastrobin Chemical Properties
Melting point 97~101℃
density 1.16±0.1 g/cm3(Predicted)
solubility DMSO (Slightly), Methanol (Slightly)
pka11.26±0.46(Predicted)
form Solid
color White to off-white
BRN 11330196
Henry's Law Constant2.9×105 mol/(m3Pa) at 25℃, Ebert et al. (2023)
Major Applicationagriculture
environmental
InChI1S/C18H25N5O5/c1-12(20-25-4)16(22-26-5)13(2)21-28-11-14-9-7-8-10-15(14)17(23-27-6)18(24)19-3/h7-10H,11H2,1-6H3,(H,19,24)/b20-12+,21-13+,22-16+,23-17+
InChIKeyJHIPUJPTQJYEQK-ZLHHXESBSA-N
SMILESCNC(=O)C(=N\OC)\c1ccccc1CO\N=C(C)\C(=N\OC)\C(C)=N\OC
Safety Information
Hazard Codes Xn,N
Risk Statements 20/22-40-50/53
Safety Statements 22-36/37-46-61
RIDADR UN 3077 9 / PGIII
WGK Germany 3
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Inhalation
Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Carc. 2
MSDS Information
Orysastrobin Usage And Synthesis
DescriptionOrysastrobin is a rice fungicide. It has a moderate aqueous solubility, is volatile and, based on its chemical properties, is mobile and can be expected to leach to groundwater. It is generally moderately persistent in soil systems but will not usually persist in aquatic systems under certain conditions. It is not generally susceptible to hydrolysis. It has a moderate mammalian toxicity and has a high potential to bioaccumulate. It is moderately toxic to most aquatic species, birds and earthworms but relatively non-toxic to honeybees.
UsesOrysastrobin is a fungicide used in the treatment of blast and sheath blight in transplanted rice inhibiting the mitochondrial respiration chain.
DefinitionChEBI: A monocarboxylic acid amide obtained by formal condensation of the carboxy group of (2E)-(methoxyimino){2-[(3E,5E,6E)-5-(methoxyimino)-4,6-dimethyl-2,8-dioxa-3,7-diazanona-3,6-dien-1-yl]ph nyl}acetic acid with the amino group of methylamine. A rice fungicide that is highly effective against Magnaporthe oryzae, Pyricularia oryzae, Thanatephorus cucumeris and Rhizoctonia solani.
Production MethodsOrysastrobin is synthesised through a multi-step chemical process involving the construction of its complex heterocyclic structure. The synthesis typically begins with the formation of a methoxyimino intermediate, which is then coupled with a substituted benzene ring containing a dioxa-diazanonadiene moiety. This key intermediate undergoes further condensation with N-methylacetamide under controlled conditions to form the final active compound. The reaction sequence involves precise temperature control, solvent selection and purification steps such as crystallisation or chromatography to ensure high purity.
Mechanism of actionSystemic, broad-spectrum with protective and curative properties. Interferes with the respiration process. Respiration inhibitor (QoL fungicide).
Pesticide TypeFungicide
Orysastrobin Preparation Products And Raw materials
Tag:Orysastrobin(248593-16-0) Related Product Information
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