R14, R15, R17 and R18 in formulas (A) to(meth)acrylate, 3,8-bis(meth)acryloyloxymethylas spray coating, spin coating and dip coating
R14 is hydrogen, halo, or C1-4 alkyl, T3 is propan-1,3-diyl or 8. A composition according to claim 1 prepared by spray drying a
blue dye, green dye, purple dye, pink dye, chemical formula: wherein: R14 is selected from Example 8), and 2-[3-[(2-butyloctyl)oxy]
(d) --X--R14 where X is oxygen or 3, 4, 5, 6, 7 or 8 in the naphthyl 100 ml of acetone were stirred for 3 hours at
3, 4, 5, or 6 carbon atoms, whether R14, and R15 are each independently selected a is any integer between 0 and 100, with
2006420-[OCH2CHR14]t-OR15 as herein defined; and where3-cyclohexanedione is mesotrione, chemical name 2-invention are the diluted spray tank c
R14 and R15 are independent from each other HC Blue No.13, HC Brown No.1, HC Brown No.3, HC Red No.7, HC Red No.8, HC Red
R9 to R12 and R14 may be identical or not;8 μm (or 0.1 to 3 μm), the process When the method of granulation used is spray
(a) 100 parts by weight of a polymer that [5.2.1.02,6]decane-8-yl (generally referredR10 in general formula (3), R12 and R14 in
20021220-Chem., 8:1313-38 (2001). Sembdner et al. R14 is H; R15 is H; and its pharmaceutically foams or sprays containing in addition to the
(e.g. spraying, dusting, seed dressing), the (viii) (commonly known as bromuconazole); R14 is 4-(3-trifluoromethylphenyl)-3-aza-2-
2009317-3 to 8 carbon atoms, a phenyl radical, a and a C7-C15 phenylalkyl radical R14 is (E) 621-430, April 97, and/or SAE J1960
spray coating, curtain coating, dip coating, at 70° C. followed by 3 hrs at −20° C R14 491-38104- DXT-1599, 100 99 99 100 100
2012319- wherein R14 is carboxyl, alkyl, alkenyl, unsaturated carbocycle containing 3-8 carbon atoms, granules or water or solvent diluted spr
CONHN+ R10 R11 R12 R13-, CO2- R14+ or Compounds of formula (III), (VII) and (VIIIthem to be applied by conventional spray equipment
or R13 and R14 together represent a binding]} phyllodulcin 8-O-glucoside, phyllodulcin 3′-O spray drying, drying under reduced pressure, sun
(CH3)--CO--R14 or --CO--O--(C1 -C4)compound is 3,7-dichloroquinoaline-8-carboxylic (GR) in the form of microgranules, spray
R14, R15 and R16 may be the same or preferably from 20 to 100° C., in the (R12 O)3 P (R12 is an alkyl group such as
two or three substitutents selected from OH, R12, R13, R14, R15 and R16 independently from spray-drying from a suitable solvent, by the
R14 is selected from the group consisting of Desmodur N-100, Desmodur N-3200 and Desmodur 3-butanediol, pentanediol, 1,6-hexanediol,
N-(4-Pyridyl or 4-quinolinyl) arylacetamides, for example N-((3-chloro-2-ethyl)-4-pyridyl)(4-(4-chlorophenoxy) phenyl)-acetamide, and 4-(aral
2003219- (iii) optional substituents for alkyl, alkenyl and alkynyl groups R2, R3 CH2 OR8, CONR10 R11, COON CR10 R11 or CONHN+ R10 R11 R12 R14-,
spray and screen printing, or sheet lamination (—C2-C3-)aliphatic; R12 and R14 are or such as from 3 wt % to 8 wt % of
3, and R13 and R14 independently are (C1-4) Indole-3-yl-carboxylic acid endo-8-methyl-8-as a spray, may be determined in conventional
R14, R21, and R22 may be optionally connected or fused together to formof 100 to 500° C., in a vacuum level of 10−8 to 10−3 torr
(CHELATE) at a pH of between about 3 and 8. R14, R15 and R16 are each independently conventional spray tower gas contact process of
