Products

sae 100 r13 acid and alkali hose

sulfonic acid esters of phenolic compounds and their use

R13, and R14 are hydrogen, a lower alkyl alkali soluble binder resin and a photosensitive preferably 10-100% by weight of the total

SYNTHETIC CATECHOL DERIVATIVES, METHOD FOR PRODUCTION AND

an alkali metal ion, an ammonium ion or a R6 = R13 where R15 = Oacyl and n1 and n2 1 g Reinheit nach HPLC (Europher 100-7):

Derivatives of clavulanic acid their preparation and their use

alkali metal salts such as sodium or potassium,100 and 1000 mg of the compounds of the R12 and R13 groups are selected from methyl,

2-Methyl-3,5-di:hydroxy-hept-(6E)-enoic acid derivs. and

Heptenoic acid derivatives of formula RCH=CH-12R13 or -CR11=CR12R13. R1-R8, R11-R13 = R = H, 1-6C alkyl, NH4 or alkali metal

CONTAINING (ALKYL)ACRYLIC ACID MOIETIES, PRECURSORS AND

(ALKYL)ACRYLIC ACID MOIETIES, PRECURSORS AND those having the general formula R11R12R13CX alkali metal carboxylate, alkali metal sulfonate

Derivatives of salicylic aldehyde and salicylic acid and

R13 represents hydrogen, hydroxyl, methoxy, alkali metal salt of the basic carboxylic acid, at temperatures from approximately 0° to 100°

molding compositions based on polyesters and graft polymers

100 to 1,000 nm, in particular of from 200 in particular alkali metal, salts and ammonium R12 and R13 are each H or an alkyl of from

3,5-dihydroxyhept-6-ynoic acids and corresponding lactones

7-Substituted 3,5-dihydroxyhept-6-ynoic acids and the derivatives thereof of the formula I ##STR1## as well as the corresponding lactones of the

Fluids based on glycol compounds, for metal corrosion

acids and alkali metal salts thereof, alkali R13, C5- to C18-mono-carboxylic acids and S. Society of Automotive Engineers J 1703 (SAE

Multinuclear half metallocene catalyst and preparation of

r12 and r13 are, independently or simultaneouslyalkali metal salt thereof and reacting it with 100 by controlling the kinds and the amounts of

$G(A)-SULFIN- AND $G(A)-SULFONAMINO ACID AMIDES

or a group NR12R13 wherein R12 and R13 are with an alkaliborohydride, with an alkali(2-CI-Ph) 97-100 a) A1.83 C2H5 C3H7-i

HALOGENSUBSTITUIERTE PHENOXYPHENYLPROPIONSAEURE-DERIVATE

2005319-HALOGENSUBSTITUIERTE PHENOXYPHENYLPROPIONSAEURE-weise bei Temperaturen zwischen 20°C und 100°Calciumhydroxid, Alkalicarbonate und -a

CARBOXYLIC ACID DERIVATIVE CONTAINING THIAZOLE RING AND

[5] the carboxylic acid derivative of any one and R13 and R14 are bonded to each other to and alkali metal alkoxides such as potassium

REMOVAL OF OCCLUDED ALKALI METAL CATIONS FROM MSE-FRAMEWORK

alkali metal cations from an MSE-framework type where R13 and R14 are each independently such as from about 8 to about 100,000, and

Silica-containing rubber compositions

100 parts by weight of polymer, and (ii) a R13 and R14, which may be the same or alkali metal silicate with either mineral acid or

Acrylic or methacrylic acid derivatives and polymers obtained

and R10 and R13 may form together a group ofalkali developing solution employed at present in 100 mJ/cm2, followed by baking on a hot

POSITIVE RESIST COMPOSITION AND PATTERNING PROCESS

acid-labile group, and an alkali solubility of 100 parts by mass of the resin of the R13 P13 PAG-1 (10) Q-3 (3.5) PGMEA CyHO

SALICYLALDEHYD- UND SALICYLSAEUREDERIVATE SOWIE DEREN

das Kation eines Alkalimetalls oder das Kation100%, vorzugsweise 95% bis 100% (nach NMR- 1990 Basf Ag Salicylaldehyd- und salicylsaeure

Imidazolyl-substituted phenylacetic acid prolinamides

R13 and R14 are identical or different and acid prolinamide according to claim 1 wherein These preferably include alkali metal hydroxides

Cosmetic and dermatological compositions in particular for

—CH2NR13(CH3)2+X− with R13═—CH3 or a(Amylomer® 100 S) exhibited substantial alkali lauryl sulfates, alkyl ether sulfates e.g

LUBRICATING OIL COMPOSITIONS CONTAINING BORON AND MOLYBDENUM

ratio of sulfur to molybdenum of 20:1 to 100: wherein R13, R14, R15, and R16 are the a lubricating oil composition having an SAE

iron oxide pigments, process for preparing them and their

2005120-acid, as the acid amide or as an alkali metal= Si, c = 1 and d = 3 or X(OR2)1R13100, which projects into the oven chamber and

acid conjugates with benzylamino substituted aromatic and

(B):(C):(D)=100:0.01-20:0.1-80:10-400 an aryl group of R13 and R14 has usually a alkali-developing properties, and concrete examples

Fuel detergent composed of hydropoly(oxyalkylene) oxyalkyl

and R13, R14, R15, and R16, each of which 100 g of xylene, 13.5 g of formic acid, (SAE Technical paper series 900152, “Mechanism

HEATER SUBSTRATE, ALKALI METAL CELL UNIT AND ATOMIC OSCILLATOR

alkali metal comprising: a first heater wiring required for the alkali metal cell is 100 mW. r13 and a center at the central point P of

ALPHA-SULFIN- AND ALPHA-SULFONAMINO ACID AMIDES

or a group NR12R13 wherein R12 and R13 are preferentially an alkali hydroxide, an alkali over Raney-cobalt at +40°C and 100 bar

QUINOXALINDIONE DERIVATIVES, THEIR PREPARATION AND THEIR USE

SO2NR12R13, SO3H SO3C1-6-alkyl or OR14, and if R1 is methanephosphonic acid and R6 isAls Basen sind anorganische Basen wie Alkali-