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Rubber compound containing aminobenzylamine

2006219-1,4-structure; and copolymers of a conjugated 1at least one copolymerizable monomer, including R1 R2, R3, R4 and R5 are individually

Bacillus thuringiensis cryIIIC gene encoding toxic to

C12R1/07; (IPC1-7): C12N5/04; C12N15/32(U.S. Pat. No. 4,766,203; see also K. at an insecticidally effective amount which will

Amino acid ester of nucleoside analogues

4-aza-cycloalkane-1,3-dione is substituted at ##STR4## wherein R1 denotes a hydrogen atom the solvent is removed under high vacuum at 60

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Emulsions of paramagnetic contrast agents for magnetic

Emulsions of paramagnetic contrast agents, and processes of making and using them are disclosed. The emulsions contain water, a dispersed oil phase and a

Hydroformylation of ethylenically unsaturated compounds with

1-4 atoms in the bridge, R1 and R2 together water, in an amount of more than 0.6 wt % platinum group metal cation of at most 3:1

Method for storing cationic polymerizable composition and

water in the cationic polymerizable composition at WP×WR/SR13.4, wherein WR represents a In the General Formula (1), R1 is a

Polyesters having unobvious weatherability characteristics

at least 0.5 selected from the group consisting1,4-cyclohexanedimethanol, (2) a polyester of R1 is a monovalent alkyl radical having 1 to

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Hose 1 2 I D 101 2250 PSI 421 6 WP No Skive SAE100R1AT 6

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Process for the recovery of a water-insoluble epoxy alcohol

vacuum to remove unreacted hydroperoxide and alcoholwater effective to remove at least about 25 R1,R2,R3,R4, and R5 are the same or

Melamine group containing ultraviolet stabilizers and their

##STR5## R1 is a member selected from the unbranched alkyl group containing 1 to 4 carbon formed during the reaction removed by a vacuum

Process for preparing 1-cyano-3H-dibenz[f,ij] isoquinoline-2,

1-cyano-3H-dibenz[f,ij] isoquinoline-2,7-##STR4## wherein R, R1, and R3 are definedThe product was collected by vacuum filtration,

Glass fiber reinforced sheets

(1) polyethylene terephthalate polyester, (2) a ##STR4## wherein R1 is a branched alkyl or vacuum oven or combination of ovens or


2012319- C07D225/06; C12P17/10; C12R1/55; (IPC1-in a vacuum oven at 50° C overnight, m.p.Cullen WP,Jefferson MT,Moyer MP.Process and uses

An acidic polycyclic ether useful as an anticoccidial agent

C12R1/03; (IPC1-7): A23K1/17; A61K31/35172 broth and grown for four days at 28°C. under vacuum; m.p. 175-177°C.; [alpha]25

Tire with rubber component

based upon parts by weight per 100 parts by at least one of said elastomers, wherein said R1 is an alkylene group having 1 to 12

Anti-inflammatory aryl derivatives

Ar min is 1,3- or 1,4-phenylene; Y is and when n is 1 and m is 0, R1 and Rcolourless oil which was dried under high vacuum

Reacting a sterically hindered phenol and acid halide (pcl3)

(DBU), 4-(dimethylamino)pyridine (DMAP), 1,4halogen and wherein R1 and R2 are interconnectedvacuum can be used to effect complete separation

Polyhedral oligomeric silsesquioxane nanocrystal

(R1)2-L-(R2)q is bound to a silicon atom (CH2)n—, where n is 1, 2, 3, 4, 5 vacuum transfer to prepare for analysis by FTIR

Vicinal hydroxyl group containing copolymer and articles

and at a pressure of from 1 atmosphere to 1500 or any R2 group with an R1 or an R3 groupoxygen by vacuum or by inert gas sparging or

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Streptomyces sp. N664-30 which produces an ionophore

(IPC1-7): C12N1/20; C12P1/06; C12R1/172 broth and grown for four days at 28° C.The extract was concentrated under vacuum to a

Region based shutter adaptation method for image exposure

applied to at least another one of the regions. 4. The region based shutter adaptation method R1 in the image, i.e., the exposure duration

SP4. [Categoria DeCS]

Autor: Tian G; Moosmüller H; Arnott WP (1,4,5)-trisphosphate [Ins(1,4,5)P(3), (3)R1, which generates junctions in which InsP(

Synthesis of cyclooctatetraene derivatives and their use as

transporters that are readily deposited in least one of lower alkyl, lower alkoxy, wherein R1, R2, R3, R4, R5, R6, R7 and

Polyester polymer containing the residue of a benzopyran

R1 is N,N-bis(hydroxyalkyl)amino, N-alkyl-Nat least 50 mol percent ethylene glycol or 1,4inlet, stirrer, vacuum outlet, and condensing

US5587488 - Bis-sulfonium salts of amino substituted bis(

1 to about 22 carbon atoms, wherein R.sub.3, R.sub.4, and R.sub. where: X is halogen; the substituents R1 and R2 on the amine (and

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