Iprobenfos
- CAS No.
- 26087-47-8
- Chemical Name:
- Iprobenfos
- Synonyms
- epb;EBP;IBP;ricidp;C15230;ricidii;KITAZIN;kitazinl;KITAZINE;Kitazin L
- CBNumber:
- CB4298968
- Molecular Formula:
- C13H21O3PS
- Molecular Weight:
- 288.34
- MOL File:
- 26087-47-8.mol
- MSDS File:
- SDS
- Modify Date:
- 2025/1/21 19:06:49
Melting point | 25°C |
---|---|
Boiling point | 126°C |
Density | 1.1001 g/cm3 |
vapor pressure | 2.5 x 10-4 Pa (20 °C) |
refractive index | approximate 1.51 |
Flash point | 11 °C |
storage temp. | APPROX 4°C |
Water Solubility | 430 mg l-1(20 °C) |
form | liquid |
biological source | rabbit |
BRN | 1974687 |
CAS DataBase Reference | 26087-47-8(CAS DataBase Reference) |
NIST Chemistry Reference | Kitazin p(26087-47-8) |
EPA Substance Registry System | Phosphorothioic acid, O,O-bis(1-methylethyl) S-(phenylmethyl) ester (26087-47-8) |
SAFETY
Risk and Safety Statements
Symbol(GHS) | GHS07,GHS09 |
---|---|
Signal word | Warning |
Hazard statements | H302-H411 |
Precautionary statements | P264-P270-P273-P301+P312-P391-P501 |
Hazard Codes | Xn;N,N,Xn,T,F |
Risk Statements | 22-51/53-39/23/24/25-23/24/25-11 |
Safety Statements | 61-45-36/37-16-7 |
RIDADR | UN 3082 |
WGK Germany | 2 |
RTECS | TE6550000 |
HazardClass | 6.1(a) |
PackingGroup | II |
HS Code | 29309090 |
Iprobenfos Chemical Properties,Uses,Production
Uses
Iprobenfos is a systemic fungicide which provides effective protective and curative control of leaf and ear blast (Pyricularia oryzae), stem rot (Helminthosporium spp.) and sheath blight (Rhizoctonia solani) in rice.
Definition
ChEBI: An organic thiophosphate that is the S-benzyl O,O-diisopropyl ester of phosphorothioic acid. Used as a rice fungicide to control leaf and ear blast, stem rot and sheath blight.
Metabolic pathway
Iprobenfos undergoes extensive degradation and metabolism. Primary metabolic pathways include isomerisation to the thionate (P=S) ester, cleavage of the P-S-benzyl and P-O-isopropyl moieties, and transesterification. Benzyl mercaptan, upon cleavage, undergoes additional oxidation reactions to yield the alcohol, carboxylic acid, disulfide and sulfonic acid. The formation of the oxon from the isomerisation product (P=S ester) was minor and was observed only under UV light irradiation. The primary metabolic pathways of iprobenfos are presented in Scheme 1.
Iprobenfos Preparation Products And Raw materials
Raw materials
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chevron_rightPreparation Products
Supplier | Tel | Country | ProdList | Advantage | Inquiry |
---|---|---|---|---|---|
Pharmaffiliates Analytics and Synthetics P. Ltd | +91-172-5066494 | Haryana, India | 6739 | 58 | Inquiry |
SynZeal Research Pvt Ltd | +1 226-802-2078 | Gujarat, India | 6514 | 58 | Inquiry |
Sai Sheti Seva Kendra | 08068441170Ext 344 | Maharashtra, India | 1 | 58 | Inquiry |
Mauli Agro Services | 08068441028Ext 206 | Maharashtra, India | 1 | 58 | Inquiry |
PI Industries Limited | 08048372067Ext 754 | Haryana, India | 7 | 58 | Inquiry |
Agri Care | 08048372668Ext 708 | Nagpur, India | 1 | 58 | Inquiry |
Pharma Affiliates | 172-5066494 | Haryana, India | 6754 | 58 | Inquiry |
career henan chemical co | +86-0371-86658258 +8613203830695 | China | 29879 | 58 | Inquiry |
Chongqing Chemdad Co., Ltd | +86-023-6139-8061 +86-86-13650506873 | China | 39894 | 58 | Inquiry |
CONIER CHEM AND PHARMA LIMITED | +8618523575427 | China | 49374 | 58 | Inquiry |
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