Cas no 187166-40-1 (Spinetoram-J)

Spinetoram-J is a semi-synthetic insecticide derived from the fermentation of Saccharopolyspora spinosa, belonging to the spinosyn class of compounds. It exhibits broad-spectrum activity against lepidopteran and other pest species by targeting nicotinic acetylcholine receptors, leading to rapid paralysis and mortality. The product is characterized by its favorable environmental profile, including low mammalian toxicity and minimal impact on non-target organisms such as pollinators and beneficial insects. Its unique mode of action reduces the risk of cross-resistance with other insecticide classes. Spinetoram-J is effective at low application rates, providing durable crop protection while supporting integrated pest management (IPM) programs.

Spinetoram-J structure

Product Name:Spinetoram-J

CAS No:187166-40-1

MF:C₄₂H₆₉NO₁₀

MW:747.997974157333

CID:2170843

PubChem ID:24795086

Update Time:2025-10-30

Spinetoram-J Chemical and Physical Properties

Names and Identifiers

- Spinetoram
- Spinetoram (major component)
- 3'-Ethoxy-5,6-dihydrospinosyn J
- Spinetoram (major component) [iso]
- spinosyn J, 3'-Ethoxy-5,6-dihydro-
- SPINETORAM, 10ΜG
- μL in acetonitrile
- GOENIMGKWNZVDA-RWGFPKGXSA-N
- 935545-74-7
- 1H-as-Indaceno[3,2-d]oxacyclododecin-7,15-dione, 2-[(6-deoxy-3-O-ethyl-2,4-di-O-methyl-.alpha.-L-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,4,5,5a,5b,6,9,10,11,12,13,14,16a,16b-hexadecahydro-14-methyl-, (2R,3aR,5aR,5bS,9S,13S,14R,16aS,16bR)-
- 2HRU6LA8S5
- UNII-2HRU6LA8S5
- (1S,2R,5R,7R,9R,10S,14R,15S,19S)-15-[(2R,5S,6R)-5-(dimethylamino)-6-methyloxan-2-yl]oxy-7-[(2R,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyloxan-2-yl]oxy-19-ethyl-14-methyl-20-oxatetracyclo[10.10.0.02,10.05,9]docos-11-ene-13,21-dione
- C42H69NO10
- Spinetoram J
- Spinetoram; DE 175J; Spinetoram J
- Spinetoram 10 microg/mL in Acetonitrile
- DTXSID3052854
- Spinetoram-J
- 1ST20631
- SpinetoramJ
- 187166-40-1
- Q27254760
- XDE-175-J
- SCHEMBL678137
- Spinetoram, 10 μg /μL in acetonitrile
- 1H-as-Indaceno(3,2-d)oxacyclododecin-7,15-dione, 2-((6-deoxy-3-O-ethyl-2,4-di-O-methyl-alpha-L-mannopyranosyl)oxy)-13-(((2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl)oxy)-9-ethyl-2,3,3a,4,5,5a,5b,6,9,10,11,12,13,14,16a,16b-hexadecahydro-14-methyl-, (2R,3aR,5aR,5bS,9S,13S,14R,16aS,16bR)-
- 1H-as-Indaceno[3,2-d]oxacyclododecin-7,15-dione, 2-[(6-deoxy-3-O-ethyl-2,4-di-O-methyl-alpha-L-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,4,5,5a,5b,6,9,10,11,12,13,14,16a,16b-hexadecahydro-14-methyl-, (2R,3aR,5aR,5bS,9S,13S,14R,16aS,16bR)-
- (1S,2R,5R,7R,9R,10S,14R,15S,19S)-15-((2R,5S,6R)-5-(dimethylamino)-6-methyloxan-2-yl)oxy-7-((2R,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyloxan-2-yl)oxy-19-ethyl-14-methyl-20-oxatetracyclo(10.10.0.02,10.05,9)docos-11-ene-13,21-dione
- 803-245-9
- DTXCID2032055
- Inchi： 1S/C42H69NO10/c1-10-27-13-12-14-35(53-37-18-17-34(43(6)7)24(4)49-37)23(3)38(45)33-21-31-29(32(33)22-36(44)51-27)16-15-26-19-28(20-30(26)31)52-42-41(47-9)40(48-11-2)39(46-8)25(5)50-42/h21,23-32,34-35,37,39-42H,10-20,22H2,1-9H3/t23-,24-,25+,26-,27+,28-,29-,30-,31-,32+,34+,35+,37+,39+,40-,41-,42+/m1/s1
- InChI Key： GOENIMGKWNZVDA-RWGFPKGXSA-N
- SMILES： O([C@H]1[C@@H]([C@@H]([C@H]([C@H](C)O1)OC)OCC)OC)[C@@H]1C[C@H]2CC[C@H]3[C@@H]4CC(=O)O[C@@H](CC)CCC[C@@H]([C@@H](C)C(C4=C[C@H]3[C@@H]2C1)=O)O[C@H]1CC[C@@H]([C@@H](C)O1)N(C)C

Computed Properties

Exact Mass: 747.49214740g/mol
Monoisotopic Mass: 747.49214740g/mol
Isotope Atom Count: 0
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 11
Heavy Atom Count: 53
Rotatable Bond Count: 10
Complexity: 1260
Covalently-Bonded Unit Count: 1
Defined Atom Stereocenter Count: 17
Undefined Atom Stereocenter Count : 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
XLogP3: 5.9
Topological Polar Surface Area: 111?2

Spinetoram-J Pricemore >>

Related Categories	No.	Product Name	Cas No.	Purity	Specification	Price	update time
TRC	S683650-1mg	Spinetoram-J	187166-40-1		1mg	$ 176.00	2023-09-06
TRC	S683650-10mg	Spinetoram-J	187166-40-1		10mg	$ 1401.00	2023-09-06
BioAustralis	BIA-E1583-1mg	spinosyn J, 3′-Ethoxy-5,6-dihydro-	187166-40-1	>95% by HPLC	1mg	$300.00	2025-07-04
BioAustralis	BIA-E1583-5mg	spinosyn J, 3′-Ethoxy-5,6-dihydro-	187166-40-1	>95% by HPLC	5mg	$1050.00	2025-07-04
BioAustralis	BIA-E1583-1 mg	spinosyn J, 3′-Ethoxy-5,6-dihydro-	187166-40-1	>95%byHPLC	1mg	$304.00	2023-09-14
BioAustralis	BIA-E1583-5 mg	spinosyn J, 3′-Ethoxy-5,6-dihydro-	187166-40-1	>95%byHPLC	5mg	$1064.00	2023-09-14
A2B Chem LLC	AE99589-20mg	SPINETORAM	187166-40-1		20mg	$815.00	2024-04-20

Spinetoram-J Suppliers

Suzhou Senfeida Chemical Co., Ltd

Gold Member

Audited Supplier

(CAS:187166-40-1)SPINETORAM

Order Number:sfd20587

Stock Status:in Stock

Quantity:200kg

Purity:99.9%

Pricing Information Last Updated:Friday, 19 July 2024 14:38

Price ($):discuss personally

Email:[email protected]

Product Official Link

Tiancheng Chemical (Jiangsu) Co., Ltd

Gold Member

Audited Supplier

(CAS:187166-40-1)Spinetoram-J

Order Number:LE15551

Stock Status:in Stock

Quantity:25KG,200KG,1000KG

Purity:99%

Pricing Information Last Updated:Friday, 20 June 2025 12:12

Price ($):discuss personally

Email:[email protected]

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Additional information on Spinetoram-J

Spinetoram-J: A Comprehensive Overview

Spinetoram-J, identified by the CAS number 187166-40-1, is a compound that has garnered significant attention in recent years due to its unique properties and potential applications across various industries. This compound, classified under the broader category of organophosphates, has been extensively studied for its role in pest control, agricultural practices, and other specialized uses. The latest research on Spinetoram-J has shed light on its efficacy, environmental impact, and potential for further development.

The chemical structure of Spinetoram-J is characterized by its phosphate ester group, which plays a crucial role in its functionality. Recent studies have highlighted the compound's ability to inhibit specific enzymes, making it highly effective in controlling pests without causing significant harm to non-target species. This selective action has made it a preferred choice in integrated pest management (IPM) strategies, particularly in agriculture and horticulture.

In terms of application, Spinetoram-J has been widely used in crop protection due to its rapid knockdown effect on target pests. Field trials conducted in various regions have demonstrated its effectiveness against a wide range of insects, including those resistant to traditional pesticides. The compound's ability to degrade quickly in the environment further enhances its appeal as an eco-friendly solution compared to older generations of pesticides.

Recent advancements in the synthesis of Spinetoram-J have focused on improving yield and reducing production costs. Researchers have explored alternative synthetic pathways that minimize the use of hazardous intermediates, aligning with global trends toward sustainable chemistry practices. These innovations not only enhance the commercial viability of the compound but also contribute to safer working conditions in manufacturing facilities.

The environmental impact of Spinetoram-J has been a focal point of recent studies. While it is effective in pest control, concerns about its persistence in soil and water systems have led to stricter regulations on its application rates and usage patterns. Regulatory bodies are now encouraging farmers and applicators to adopt best management practices (BMPs) to mitigate any potential risks associated with this compound.

In addition to its agricultural applications, there is growing interest in exploring the medical potential of Spinetoram-J. Preliminary research suggests that it may have therapeutic properties, particularly in targeting specific enzymes involved in disease pathways. However, further studies are required to fully understand its pharmacokinetics and safety profile before it can be considered for clinical use.

The global market for compounds like Spinetoram-J continues to expand, driven by increasing demand for sustainable pest management solutions. Key players in the industry are investing heavily in R&D to develop new formulations and delivery systems that enhance the efficiency and safety of this compound. These efforts are expected to shape the future trajectory of pest control technologies worldwide.

In conclusion, Spinetoram-J, with its CAS number 187166-40-1, represents a significant advancement in pest control chemistry. Its unique properties, combined with ongoing research into its applications and environmental impact, position it as a critical component of modern agricultural practices. As technology continues to evolve, so too will our understanding of this compound's potential benefits and challenges.

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