IP Library › Granted Patent US 10,005,754
Granted Patent B2
US 10,005,754 · App. 14/967,950 · Granted Jun 26, 2018

Form of spirodiclofen, a process for its preparation and use the same

Inventor: James Timothy Bristow (Chai Wan, HK)
Assignee: ROTAM AGROCHEM INTERNATIONAL COMPANY LIMITED
C07D307/94A01N25/04A01N43/12C07B2200/13
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Quick Facts
Patent No.
US 10,005,754
App. No.
14/967,950
Granted
Jun 26, 2018
Kind
B2
Abstract

A new crystalline form of spirodiclofen of formula (I), the crystal preparation process, the analyzes of the crystal through various analytical methods and using the crystal to prepare stable agrochemical formulation. The invention also describes the use of various solvents towards the crystalline form preparation conditions.

Claims (27)

1. A crystalline modification I of spirodiclofen (3-(2,4-dichlorophenyl)-2-oxo-1-oxaspiro[4.5]dec-3-en-4-yl-2,2-dimethylbutyrate), exhibiting each of the following reflexes as 2θ values in an X-ray powder diffractogram recorded using Cu—Kα radiation at 25° C.:

2θ=11.322±0.2  (1)

2θ=14.858±0.2  (2)

2θ=15.382±0.2  (3)

2θ=17.184±0.2  (4)

2θ=19.617±0.2  (5)

2θ=22.784±0.2  (7)

2θ=23.840±0.2  (8)

2θ=25.725±0.2  (9).

2. The crystalline modification I of spirodiclofen according to claim 1 , exhibiting each of the following reflexes in an X-ray powder diffractogram recorded using Cu—Kα radiation at 25° C.:

2θ=11.322±0.2  (1)

2θ=14.858±0.2  (2)

2θ=15.382±0.2  (3)

2θ=17.184±0.2  (4)

2θ=19.617±0.2  (5)

2θ=21.739±0.2  (6)

2θ=22.784±0.2  (7)

2θ=23.840±0.2  (8)

2θ=25.725±0.2  (9)

2θ=28.195±0.2  (10).

3. The crystalline modification I of spirodiclofen according to claim 1 , exhibiting an IR spectrum with characteristic functional group vibrations peaks at wavenumbers (cm −1 , ±0.2%) of one or more of about 2971, 2928, 2854, 1780, 1749, 1096, 1061, 862, and 819 cm −1 .

4. The crystalline modification I of spirodiclofen according to claim 1 exhibiting a Differential Scanning calorimeter (DSC) thermogram having an endothermic melting peak with onset at about 98.6° C.

5. A crystalline material comprising the crystalline modification I of spirodiclofen according to claim 1 , wherein the crystalline modification I of spirodiclofen is obtained using a solvent, the solvent is toluene, and the crystalline material having a content of the crystalline modification I of spirodiclofen of at least 98% by weight.

6. A composition comprising the crystalline modification I of spirodiclofen according to claim 1 and at least one auxiliary.

7. The composition according to claim 6 , wherein the auxiliary is selected from the group consisting of a surfactant, a diluent, a wetting agent, a dispersant, a thickening agent, an antifoaming agent, an anti-freezing agent, a preservative, an antioxidant, a solid adherent, an inert filler and mixtures thereof.

8. The composition according to claim 6 , in the form of a suspension concentrate (SC), an oil-based suspension concentrate (OD), a water-soluble granule (SG), a dispersible concentrate (DC), an emulsifiable concentrate (EC), an emulsion seed dressing, a suspension seed dressing, a granule (GR), a microgranule (MG), a suspoemulsion (SE) or a water-dispersible granule (WG).

9. The composition according to claim 8 , in the form of a suspension concentrate (SC).

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2017
From: BRISTOW, JAMES TIMOTHY
To: ROTAM AGROCHEM INTERNATIONAL COMPANY LIMITED
Reel/Frame 044969/0142 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2016
From: BRISTOW, JAMES TIMOTHY
To: ROTAM AGROCHEM INTERNATIONAL COMPANY LIMITED
Reel/Frame 038141/0768 →
Continuity (1)
Related Publication 20170166546A1 · Jun 15, 2017