Abstract:
A curing agent (A) for resins (B) which can be cured by means of isocyanates, which has an amine number of 20 to 150 mg of KOH/g and an OH number of not more than 20 mg of KOH/g and which contains per molecule at least two masked isocyanate groups which are reactive under the conditions of curing, obtained by reacting(a) an amine which contains at least one .beta.-hydroxylalkyl group per molecule and has an OH number of 100 to 1,200 mg of KOH/g and an amine number of 100 to 1,200 mg of KOH/g and which, if appropriate, also contains NHCO groups, if appropriate as a mixture with another OH-functional and/or NH-functional compound, with(b) a partly masked isocyanate, if appropriate as a mixture with an at least difunctional, OH-reactive and/or NH-reactive compound.These curing agents are readily dispersible in aqueous systems, if appropriate after neutralization, and frequently increase stability in aqueous paint formulations.
Abstract:
Cyanohydrine derivatives of the formula ##STR1## wherein R.sub.1 and R.sub.2 are alkyl, haloalkyl, cycloalkyl, aralkyl or aryl, R.sub.3 and R.sub.4 are hydrogen, alkyl, phenyl or benzyl, R.sub.5 is hydrogen, acyl, trialkylsilyl or alkoxycarbonyl, X is oxygen or sulfur and n is zero or 1, are intermediates for the manufacture of flame retardants, bactericides, fungicides and herbicides.
Abstract:
Cyanohydrin acylates of aldehydes are manufactured by reacting aldehydes with aqueous solutions of cyanides and organic acid chlorides or anhydrides in the molar ratio of aldehyde:cyanide:acid chloride or anhydride of 1:1:1 with deviations of at most only about 10%, optionally in the presence of an inert organic solvent immiscible with water in a one-stage process. The process products are intermediates mainly in the fields of pharmaceuticals and plant protection.
Abstract:
2,5-Dioxo-1,2-oxa-phospholanes of the formula (I) ##STR1## wherein R.sup.1 is an organic radical and R.sup.2 and R.sup.3 each also represents an organic radical or hydrogen, are prepared by reacting 2-haloformylethyl-phosphinic acid halides of the formula (II) ##STR2## wherein R.sup.1, R.sup.2 and R.sup.3 are defined as in formula (I) and X means Cl or Br, preferably Cl, with an approximatey equimolar quantity of acrylic acid. The compounds (II) may also be produced in the reaction batch and in situ by reacting about equimolar quantities of a dihalophosphine of the formula (III) ##STR3## with an .alpha.,.beta.-unsaturated acid (IV)R.sup.4 -- OH (IV)In the formulae (III) and (IV) R.sup.1, R.sup.2, R.sup.3 and X are defined as indicated above.In the reaction there is formed, in addition to the compounds (I), practically exclusively .beta.-halopropionic acid and no free hydrogen halide.The phospholanes (I) are valuable flame retarding agents for plastics, intermediates, for example, for the synthesis of biocidals etc.
Abstract:
Preparation of 2,5-dioxo-1,2-oxa-phospholanes of the formula (I) ##STR1## wherein R.sup.1 represents an optionally substituted alkyl having up to 18 carbon atoms, a cycloalkyl radical having up to 8 carbon atoms, an alkylene radical having up to 8 carbon atoms, an aryl radical having up to 14 carbon atoms which may be substituted by lower alkyl groups, lower alkoxy groups, halogen or by amino groups alkylated or dialkylated by lower alkyl groups, or an aralkyl radical having up to 15 carbon atoms which may be substituted in an analogous manner as the aryl radical, R.sup.2 represents a lower alkyl radical or hydrogen and R.sup.3 represents an alkyl radical having up to 6 carbon atoms, a phenyl radical which may be substituted by halogen or by lower alkyl groups, a benzyl radical or hydrogen, by reacting 2-halogenoformylethylphosphonic acid halides of the formula (II) ##STR2## wherein R.sup.1, R.sup.2 and R.sup.3 are defined as in formula (I) and X represents chlorine or bromine, with approximately an equimolar quantity of water or one phosphinic-carboxylic acid of the formula (II), wherein both radicals X represent OH-groups.
Abstract:
2-Hydroxyethane-phosphonic acid diesters, 2-hydroxyethylphoshinic acid esters and the corresponding thiophoshonic acid-O,O-diesters or thiophosphinic acid-O-esters of the formula ##EQU1## wherein R.sub.1 is alkyl having from 1 to 18 carbon atoms, R.sub.2 has the meaning of R.sub.1 or represents cycloalkyl having up to 10 carbon atoms, alkenyl having up to 18 carbon atoms, aryl having up to 14 carbon atoms or aralkyl having up to 15 carbon atoms,R.sub.3 means hydrogen, alkyl having up to 18 carbon atoms, alkenyl having up to 18 carbon atoms, cycloalkyl having up to 10 carbon atoms, aryl having up to 14 carbon atoms or aralkyl having up to 15 carbon atoms, the substituents R.sub.1 -R.sub.3 optionally being substituted, X represents oxygen or sulfur and n represents either 0 or 1, are prepared from 2-acyloxyethane-phosphonic acid diesters, 2-acyloxy-ethyl-phoshinic acid esters or the corresponding thiophoshonic acid-O,O-diesters or thiophoshinic acid-O-esters and are important intermediate products for the preparation of plant protecting agents and flame-proofing agents.
Abstract:
A process for the preparation of phosphonic acid dihalides of the formula ##EQU1## IN WHICH R is .alpha., .beta.-unsaturated alkyl, .alpha., .beta.-unsaturated alkyl, phenyl or benzyl and may be further substituted, which comprises reacting corresponding phosphonic or pyrophosphonic acids or their functional derivatives with acid halides of the formula (CO).sub.n Hal.sub.2 where n is 1 or 2.
Abstract translation:制备式Hal RP ANGLE PARALLEL OHAL IN的膦酸二卤化物的方法R是α,β-不饱和烷基,α,β-不饱和烷基,苯基或苄基,并且可以进一步被取代,其包括使相应的膦酸或 焦磷酸或其功能衍生物与式(CO)nHal 2的酰卤反应,其中n为1或2。
Abstract:
Flame-repellant linear polyesters are obtained by incorporating by condensation phosphorus-compounds having the formula ##EQU1## wherein R and R.sub.1 are organic radicals which may also contain hereto atoms into the linear polyesters, preferably those from terephthalic acid and ethylene glycol. These polyesters are materials of which flame-repellent filaments, fibers, sheets, press-moulded and injection-moulded articles may be made. Products of the invention can be used whereever especially acute risks of ignition and fire exist.
Abstract:
Curing component (A) based on polyisocyanates for binders (B) which contain groups containing active hydrogen, wherein the curing component (A) is a product of the reaction of (a1) polyisocyanates with (a2) .alpha.-hydroxyalkylpyridines.Mixtures of (A) and (B), and also, if appropriate, diluents (C) and additives (D), are stable on storage and give, even at temperatures of 120.degree.-140.degree. C., curing products which are sufficiently solvent-stable. They are suitable, in particular, for surface-coating preparations.
Abstract:
The invention relates to aminourethanes essentially composed of structural units derived from (.alpha.) polyamines of the general formula (I) ##STR1## and of structural units derived from (.beta.) oligomeric or polymeric compounds which contain at least one terminal 2-oxo-1,3-dioxolane group.The invention further relates to a process for preparing these aminourethanes and to their use in particular in paint formulations.The aminourethanes according to the invention are suitable in particular for use as curable water-dispersible binders in particular for cationic electrocoating.