Dynamit Nobel Aktiengesellschaft

Dynamit Nobel Gmbh Explosivstoff-Und Systemtechnik

Walter Heinzelmann

Gunter Bison

Wolfgang Wolfes

Norbert Linkat

Josef Winterscheid

Kurt Breideneichen

Cornelius Ruloff

Reiner Elfgen

The present invention relates to fireproof, non-explosive solids mixtures containing nitroglycerin and anhydrous lactose that do not have to be classified as an explosive in accordance with ADR/RID, IATA, IMCO and/or UN guidelines, to methods for the preparation of such solids mixtures and to the use of anhydrous lactose for the preparation of fireproof, non-explosive solid mixtures containing nitroglycerin and lactose that do not have to be classified as an explosive in accordance with ADR/RID, IATA, IMCO and/or UN guidelines.

Fireproof, non-exploding nitroglycerine and solid mixtures containing anhydrous lactose

A gel or gel preparation of improved stability and shelf life having an action on the coronary arteries comprising nitroesters, an oil base and finely disperse silica, wherein the finely disperse silica contains hydrophilic and hydrophobic, finely disperse silica is disclosed. A method for making the gel preparation is also disclosed.

Preparation of nitroesters for coronary artery therapy

A process for the preparation of racemic phenylethylamine which comprises contacting an optical antipode therefore, e.g., L(-) or D(+)-1-phenylethylamine with sodium amide or sodium hydride.

Method of racemizing optically active 1-phenylethylamine

A process for splitting the L-(-)-.alpha.-phenylethylamine salt of D-(-)-.alpha.-azidophenylacetic acid which comprises the steps of mixing the salt with a liquid diluent and an acidic cation exchange material, effecting agitation of the resulting admixture and therefore isolating a highly purified D-(-)-.alpha.-azidophenylacetic acid. This acid product is characterized by an amine content of less than 0.2% by weight.

Process for splitting the L-(-)-.alpha.-phenylethylamine salt of

Process for producing tetrazole-1-acetic acid of maximum purity includes the steps of providing a crude reaction product containing an alkyl ester of tetrazole-1-acetic acid having from 1 to 4 carbon atoms in the alkyl group, effecting molecular distillation of this reaction product at a temperature below 130.degree.C. under a vacuum of 10.sup.-.sup.1 torr to obtain a distillant containing the alkyl ester and then gently hydrolyzing the resultant distillate to obtain the desired acid product.

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Odenthal, Germany

Walter Heinzelmann