
2009119- numsp numsp numsp R13, R14, R15, R16, R17, R18, R19 and R20alkali metal base and a metal compound with the formula MW(X)a(Y)b(Z

R13 is H or CH3; R14 is H, CJCJ alkyl, M is a alkali metal atom or an alkaline produce particles essentially all below 100 microns

weight per 100 parts by weight of said polymer;alkali-soluble by chemical change with heating ##STR11## wherein R13 is a straight-chain,

2003720-100.000 (nach dem Zahlenmittel), in der die (CO)e-R13 R13 ein beliebiger Alkyl-, Cyclo insbesondere die Alkali- und Erdalkalimetall

alkali metal compound with a compound represented R11 and R13, or R12 and R13 may together rubber composition including i) 80 to 100 phr

-NR12R13,-OCHR7-CO2R12, (C3-C6) cycloalkyl, alkali metal bicarbonates, alkaline earth metal 100% of the efficacy or phytotoxicity 1 for

2010211-50 parts by mass based on 100 parts by mass of the alkali-soluble resin When any one of R11, R12 and R13 has an aliphatic cyclic group, i

M is an alkali metal, such as Na or K, (R3)) where R3 is H or C1-C4 alkyl; R13 100 ml portion of pH 9-buffered water at

2011122-?abstract?p num=0000Die Erfindung betrifft Alkali-Aluminium-Mischphosphite der Formel (I) de-chemistryAlsub2,00/subMsubz/sub

IMIDAZOPYRIDAZINALKENSAEUREAMIDE, VERFAHREN ZU IHRER R13 für gegebenenfalls substituiertes Alkyl oder oder Alkalimetallalkyle wie Methyllithium oder

20071219- alkali metal carbonates, such as sodium carbonateR13 preferably represents straight-chain or branched(0.076 mol) of anhydrous pyridin

R11, R12, R13, R14, R15 and R16 are and ammonium or alkali metal salts of any of One hundred absorbance measurements (an average of

[0049] Examples of alkylaryl groups for R13 weight of 100 to 1,500 and preferably 200 to alkali metal salt such as a sodium salt or a

R13 and R14 independently of one another denote oxides or carbonates of the alkali metals or reaction starts from a bottom temperature of 100

A method for reducing the level of occluded alkali metal cations from an MSE-framework type molecular sieve comprises either (a) contacting the molecular

selected from the group consisting of alkali and R12 and R13 are each independently selected(100 mL) and TEA (23 mL, 165 mmol) and

and —SO2R13, wherein R8 to R13 stands alkali metal ions, earth alkali metal ions, and The ethyl acetate fraction (100 gm) was

100 microns and containing a natural or synthetic(sic) a group -SiR11R12R13, a group -P(O) alkalinising or acidifying agents or fats (sic

Alkali- und Erdalkalisalze sowie N-Methyl-glukamin, Dimethyl-glukamin, Nach Abziehen des Ethanol am Rotationsverdampfer wird dreimal mit 100 ml

2006419-substituiertes Phenyl oder -NR12R13 in Frage Alkalialkoholate (wie Natriummethanolat oder (bezogen auf 100% des eingesetzten Bindemit

(i), wherein R13 is aryl, n and s are alkali metal, hydrides of alkali metal, or 100° C. After complete dissolution, 36 g of

Natrium- oder Kaliumcarbonat, ein Alkali- oder Erdalkalimetallhydroxid wie Danach wurden 100 ml Essigester und etwas Wasser zugesetzt und die

(R13)0-3 f·ur 0 bis 3 gleiche oder vonAlkalimetallbasen wie Lithium-, Natrium- oder ·aure (98,6%) werden in 100 Teilen Wasser

and M+ is an ion of an alkali metal, an v is an integer between 0 and 100, R82, R R13, R73; R80 and/or R74; R81 together

an alkali metal cation or an ammonium cation R13 is benzyl. More preferably, the ammonium most preferably 40 to 100%, the % by weight

ethylene) using an alkali catalyst or the like.respect to 100 parts by mass of the polymer ( R12 and R13 each independently represent an

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SUBSTITUIERTE PHENYLESSIGSAEUREAMIDE German Patent oder Alkalicarbonate wie Natrium- oder Kalium+100°C, bevorzugt von +20°C bis +80°C,