WebEP0036383B1 EP81710008A EP81710008A EP0036383B1 EP 0036383 B1 EP0036383 B1 EP 0036383B1 EP 81710008 A EP81710008 A EP 81710008A EP 81710008 A EP81710008 A EP 81710008A EP 0036383 B1 EP0036383 B1 EP 0036383B1 Authority EP European Patent Office Prior art keywords esterification parts general formula … WebVerfahren zur herstellung von reiner 3,4-dichlororthanilsaeure Legal Events. Date Code Title Description; 1987-01-31: PUAI: Public reference made under article 153(3) epc to a …
Registration Dossier - ECHA
WebPrinciples of method if other than guideline: After phase separation of the test mixtures the determination of the pH-value was performed with a pH-meter with single-rod glass … WebName of test material (as cited in study report):3,4-Dichloranilin-6-sulfonsaeure (Dichlororthanilsaeure) Purity: 98.8 % (residue mainly sodium sulfate) Results and discussion. Partition coefficient Type: log Pow Partition coefficient:-1 … notifyicon windows10
Registration Dossier - ECHA - Europa
WebEs wird die Herstellung von faserreaktiven β-Sulfatoäthylsulfonyl-aminobenzaniliden durch Veresterung von β-Hydroxyäthylsulfonyl-aminobenzaniliden beschrieben. β-Hydroxyäthylsulfonyl-aminobenzanilid-Verbindungen der allgemeinen Formel in welcher die ß-Hydroxyäthylsulfonyl-Gruppe in 3'-oder 4'--Stellung des Anilidrestes gebunden ist und … WebEP0214544A2 EP86111748A EP86111748A EP0214544A2 EP 0214544 A2 EP0214544 A2 EP 0214544A2 EP 86111748 A EP86111748 A EP 86111748A EP 86111748 A EP86111748 A EP 86111748A EP 0214544 A2 EP0214544 A2 EP 0214544A2 Authority EP European Patent Office Prior art keywords acid aminonaphthalene sulfonation sulfuric … WebDE2911667A1 DE19792911667 DE2911667A DE2911667A1 DE 2911667 A1 DE2911667 A1 DE 2911667A1 DE 19792911667 DE19792911667 DE 19792911667 DE 2911667 A DE2911667 A DE 2911667A DE 2911667 A1 DE2911667 A1 DE 2911667A1 Authority DE Germany Prior art keywords hydroxynaphthalene carboxylic acid carboxylation acid … how to share bitwarden with family