Cycloxydim
- CAS No.
- 101205-02-1
- Chemical Name:
- Cycloxydim
- Synonyms
- CYCLOXIDIM;cycloxydime;FOCUS;LASER;C10913;BAS517H;STRATOS;BAS-517;an-3-yl)-;exen-1-one
- CBNumber:
- CB8474915
- Molecular Formula:
- C17H27NO3S
- Molecular Weight:
- 325.47
- MDL Number:
- MFCD01741622
- MOL File:
- 101205-02-1.mol
- MSDS File:
- SDS
| Melting point | 41℃ |
|---|---|
| Boiling point | 455.7±55.0 °C(Predicted) |
| Density | 1.21 |
| storage temp. | -20°C |
| solubility | Chloroform (Slightly), Methanol (Slightly) |
| pka | 4.32±0.25(Predicted) |
| color | White to Pale Yellow |
| BRN | 8436332 |
| Henry's Law Constant | 1.6×104 mol/(m3Pa) at 25℃, Maniere et al. (2011) |
| Stability | Hygroscopic |
| Major Application |
agriculture environmental |
| InChI | 1S/C17H27NO3S/c1-3-6-14(18-21-4-2)17-15(19)9-13(10-16(17)20)12-7-5-8-22-11-12/h12-13,19H,3-11H2,1-2H3/b18-14+ |
| InChIKey | GGWHBJGBERXSLL-NBVRZTHBSA-N |
| SMILES | CCC\C(=N/OCC)C1=C(O)CC(CC1=O)C2CCCSC2 |
| NCI Dictionary of Cancer Terms | laser |
| FDA UNII | 9NJ0YM991I |
| UNSPSC Code | 41116107 |
| NACRES | NA.24 |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS08 |
|---|---|
| Signal word | Warning |
| Hazard statements | H361d |
| Precautionary statements | P201-P308+P313 |
| PPE | Eyeshields, Gloves, type ABEK (EN14387) respirator filter |
| Hazard Codes | F,Xi,Xn |
| Risk Statements | 11-36-66-67-63 |
| Safety Statements | 9-16-26 |
| RIDADR | UN 1090 3/PG 2 |
| WGK Germany | 3 |
| RTECS | GW6425000 |
| HS Code | 29349990 |
| Storage Class | 11 - Combustible Solids |
| Hazard Classifications | Repr. 2 |
| REACH Registrations | Inactive |
Cycloxydim price More Price(8)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich | 31596 | Cycloxidim PESTANAL | 101205-02-1 | 100mg | $73.5 | 2026-04-30 | Buy |
| ChemScene | CS-0063451 | Cycloxydim 98.95% | 101205-02-1 | 5mg | $54 | 2026-06-04 | Buy |
| ChemScene | CS-0063451 | Cycloxydim 98.95% | 101205-02-1 | 10mg | $87 | 2026-06-04 | Buy |
| ChemScene | CS-0063451 | Cycloxydim 98.95% | 101205-02-1 | 25mg | $152 | 2026-06-04 | Buy |
| ChemScene | CS-0063451 | Cycloxydim 98.95% | 101205-02-1 | 50mg | $238 | 2026-06-04 | Buy |
Cycloxydim Chemical Properties, Uses, Production
Description
Cycloxydim is a systemic herbicide. It is moderately soluble in aqueous solution, is unlikely to leach to groundwater and is relatively volatile. It is not persistent in soils and is unlikely to persist in aquatic systems due to rapid aqueous photolysis. It has a low mammalian toxicity and, whilst the chemical properties suggest it may bioaccumulate, that does not appear to happen in practice. It is a skin and eye irritant. It is moderately toxic to birds, honeybees, earthworms and aquatic invertebrates. However, its is not particularly toxic to fish or other aquatic organisms.
Uses
Cycloxydim is a cyclohexene oxime herbicide that is used for the control of grass weeds of many agricultural and horticultural broad-leaved crops.
Production Methods
Cycloxydim is commercially produced through a multi-step organic synthesis. The process typically begins with the preparation of a cyclohexenone intermediate, which is then functionalised through a series of reactions including sulfonylation and oxime formation to introduce the key oxime ether moiety that characterises cycloxydim. The synthesis involves careful control of stereochemistry and reaction conditions to ensure the production of the biologically active isomer.
Definition
ChEBI: A beta-diketone that is cyclohexa-1,3-dione which is substituted at position 2 by an N-ethoxybutanimidoyl group and at position 5 by a tetrahydro-2H-thiopyran-3-yl group. A systemic herbicide effective against grasses, it is used in the cultivation of a variety of crops, including oil seed rape and potatoes.
Mechanism of action
Selective, systemic, absorbed by foliage. Acetyl CoA carboxylase inhibitor (ACCase) - distrupts fatty acid biosynthesis and lipid formation.
Metabolic pathway
Cycloxydim is rapidly metabolized in soybean plants, and four series of different types of metabolite in either free or conjugated form are identified. Transformation products are formed by chemical and/or enzymatic reactions involving a range of oxidation, a rearrangement, and cleavage of the cyclohexanone ring or ethoxyimino side chain.
Pesticide Type
Herbicide
Cycloxydim Preparation Products And Raw materials
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| J & K SCIENTIFIC LTD. | 18210857532 18210857532 | jkinfo@jkchemical.com | China | 96815 | 76 |
| Sichuan Kulinan Technology Co., Ltd | 400-1166-196 18981987031 | cdhxsj@163.com | China | 11674 | 57 |
| Chengdu Ai Keda Chemical Technology Co., Ltd. | 4008-755-333 18080918076 | 800078821@qq.com | China | 9706 | 55 |
| Nanjing Sunlida Biological Technology Co., Ltd. | 025-57798810 18652991625 | sales@sunlidabio.com | China | 3223 | 55 |
| Shanghai JONLN Reagent Co., Ltd. | 400-0066400 13621662912 | 422131432@qq.com | China | 9970 | 55 |
| Alta Scientific Co., Ltd. | 022-6537-8550 15522853686 | sales@altasci.com.cn | China | 4508 | 55 |
| Shanghai Xilong Biochemical Technology Co., Ltd. | 021-52907766-8042 | China | 9928 | 58 | |
| Shanghai YuanYe Biotechnology Co., Ltd. | 15026964105 | 2881489226@qq.com | China | 89667 | 60 |
| Raw material medicin reagent co.,Ltd | sales@njromanme.com | China | 4511 | 58 | |
| JinJin Le Chemical Co., Ltd | 18001959627(微信同号) 18001959627 | jjlchem2@163.com | China | 9890 | 58 |
