Custom Synthesis

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Custom Synthesis by ORGANICA Feinchemie GmbH Wolfen - Fine Chemicals from Wolfen - since 1910:

ORGANICA Feinchemie GmbH Wolfen is a fine chemical company, specializing in hazardous chemical reactions and focused on the exclusive synthesis of fine chemicals. ORGANICA offers the custom synthesis of advanced organic intermediates to major pharmaceutical and industrial companies around the world. 

ORGANICA is organized to be flexible and responsive to customer needs to create more value for its customers. This includes a rapid response policy to customer inquiries, direct and open customer dialogue and the ability for quick and reliable increase of production from grams to multi-tons. We continuously improve the quality and efficiency of the production process. These improvements are supported by our lean decision processes and strong in-house technical knowledge with hazardous reactions gained from over 100 years of research and production experience.

ORGANICA achieved approvals according to cGMP (current Good Manufacturing Practices) standards for some small scale products. ORGANICA is a certified ISO 9001:2008 company and takes part in the environmental project of the Chemical Industry "Responsible Care". ORGANICA is located in the ChemiePark Bitterfeld-Wolfen with its developed and cost saving infrastructure.

ORGANICA provides the custom synthesis of following products of best quality and reliability :

  • Abramovitch- Shapiro
  • Acetoacetic Ester synthesis
  • Acetylation
  • Acylation
  • Aldehyde disproportionation
  • Alder- Ene reaction
  • Aldol condensation
  • Algar- Flynn- Oyamada reaction
  • Alkoxylation
  • Alkylation
  • Allan- Robinson reaction
  • Amidation
  • Amination
  • Asymmetric synthesis
  • Baker- Venkataraman reaction
  • Balz- Schiemann reaction
  • Bamberger rearrangement
  • Bechamp reduction
  • Benzilic acid rearrangement
  • Benzoin condensation
  • Bischler quinoxaline synthesis
  • Bischler- Möhlau indole synthesis
  • Bischler- Napieralski reaction
  • Blanc cyclization
  • Blanc reaction
  • Blanc rule
  • Brackeen imidazole synthesis
  • Bredereck imidazole synthesis
  • Bromination
  • Bucherer reaction
  • Buchwald- Hartwig reactions
  • Cannizzaro reaction
  • Carbomethilation
  • Carboxylation
  • Chan- Lam Coupling
  • Chiral synthesis
  • Chlorination
  • Chloromethylation
  • Chlorosulfonation
  • Ciamician- Dennstedt rearrangement
  • Claisen condensation
  • Claisen- Schmidt reaction
  • Combes quinoline synthesis
  • Condensation
  • Conrad- Limpach reaction
  • Coumarines
  • Custom synthesis
  • Cyanation
  • Cyclysation
  • Darzens condensation
  • Darzens glycidic ester condensation
  • Darzens- Claisen reaction
  • Darzens- Nenitzescu alkylation
  • Dealkylation
  • Decarboxylation
  • Dehalogenation
  • Dehydratisation
  • Delepine reaction
  • Dess- Martin oxidation
  • Diazotation
  • Dieckmann condensation
  • Dieckmann cyclization
  • Dieckmann reaction
  • Doebner reaction
  • Doebner- von Miller reaction
  • Duff reaction
  • Einhorn variation
  • Einhorn- Brunner reaction
  • Enantiopure chemicals
  • Ene reaction
  • Eschweiler- Clarke methyIation
  • Esterification
  • Feist- Benary furan synthesis
  • Finkelstein reaction
  • Fischer esterification
  • Fischer indole synthesis
  • Fischer- Speier esterification
  • Friedel- Crafts
  • Friedel- Crafts acylation
  • Friedel- Crafts alkylation
  • Friedel- Crafts reaction
  • Friedlander quinoline synthesis
  • Fries rearrangement
  • Gabriel synthesis
  • Gabriel- Colman rearrangement
  • Gewald aminothiophene synthesis
  • Gould- Jacobs reaction
  • Gribble reduction
  • Grignard reactions
  • Grignard reagent
  • Guareschi- Thorpe condensation
  • Halogenation
  • Hantzsch pyrrole synthesis
  • Hantzsch synthesis
  • Heck reaction
  • Hell- Volhard- Zelinski reaction
  • Henry reaction
  • Heterocycles synthesis
  • Hinsberg synthesis of thiophene derivatives
  • Horner- Wadsworth- Emmons- Wittig
  • Hunsdiecker separation
  • Hydroformulation
  • Hydrogenation
  • Hydroxylation
  • Iodonation
  • Isomerisation
  • Japp- Klingemann reaction
  • Kamlet reaction
  • Knoevenagel condensation
  • Knoevenagel- Doebner condensation
  • Knorr pyrazole synthesis
  • Knorr pyrrole synthesis
  • Knorr quinoline synthesis
  • Knorr synthesis
  • Kostanecki acylation
  • Kostanecki reaction
  • Krohnke pyridine synthesis
  • Leimgruber- Batcho indole synthesis
  • Leuckart reaction
  • Leuckart reaction
  • Leuckart(-Wallach) reaction
  • Lieben haloform reaction
  • Lieben iodoform reaction
  • Madelung indole synthesis
  • Malonic ester synthesis
  • Mannich reaction
  • Methylation
  • Michael addition
  • Michael condensation
  • Michael reaction
  • Morgan- Walls reaction
  • Nencki reaction
  • Nenitzescu indole synthesis
  • Niementowski quinoline synthesis
  • Nitration
  • Nitrile synthesis
  • Nitrosation
  • Organometallic reactions
  • Oxidation
  • Paal- Knorr furan synthesis
  • Paal- Knorr pyrrole synthesis
  • Pechmann condensation
  • Pellizzari reaction
  • Perkin reaction (cinnamic acid synthesis)
  • Pfitzinger reaction
  • Pfitzner- Moffatt oxidation
  • Pharmaceutical intermediates
  • Pictet- Gams isoquinoline synthesis
  • Pictet- Hubert reaction
  • Pictet- Spengler isoquinoline synthesis
  • Piloty- Robinson pyrrole synthesis
  • Piloty- Robinson synthesis
  • Pinner reaction
  • Pomeranz- Fritsch reaction
  • Pschorr arylation
  • Quarternization
  • Reduction
  • Reductive amination
  • Reissert indole synthesis
  • Resolution of racemates
  • Sandmeyer reaction
  • Schotten- Baumann reaction
  • Scintillation dyes
  • Skraup reaction
  • Sommelet reaction
  • Steglich esterification
  • Steglich reaction
  • Stereoselective synthesis
  • Stobbe condensation
  • Sulphonation
  • Suzuki coupling
  • Swern oxidation
  • Thiele reaction
  • Thiele- Winter acetoxylation
  • Thiele- Winter reaction
  • Toll synthesis
  • Tosylation
  • Vilsmeier- Haack reaction
  • Williamson ether synthesis
  • Wittig indole synthesis
  • Wittig olefination
  • Wittig reaction
  • Wittig reagents
  • Wolff- Kishner reduction
  • Yamamoto esterification
Member of:

ORGANICA Feinchemie GmbH Wolfen
Kunstseidestr. 5
06766 Bitterfeld-Wolfen

Tel +49-3494-63-6215
Fax +49-3494-63-6165
info@organica.de
www.organica.de