Hans Fischer was a famous German organic chemist
@Chemists, Career and Childhood
Hans Fischer was a famous German organic chemist
Hans Fischer born at
In 1935, Fischer got married to Wiltrud Haufe.
On 31 March 1945, at the age of 63, Hans Fischer committed suicide in Munich in depression over the destruction of his institute and his work in the allied bombing raid during the last days of World War II.
Hans Fischer was born at Höchst am Main, Germany on July 27, 1881 to Dr. Eugen Fischer, Director of the firm of Kalle & Co, Wiesbaden, and Privatdozent at the Technical High School, Stuttgart, and Anna Herdegen.
He was initially educated in a primary school in Stuttgart, and later enrolled at the "humanistische Gymnasium" (grammar school with emphasis on the classics) in Wiesbaden from where he passed matriculation in 1899.
In 1899, he entered the University of Lausanne to study chemistry and medicine.
He was later transferred to the University of Marburg, where he graduated in chemistry under T. Zincke in 1904.
In 1906, he received a license for medicine at Munich and in 1908 Fischer qualified for his M.D. under F. von Müller at Munich.
Hans Fischer started his career at the Second Medical Clinic in Munich and at the First Berlin Chemical Institute under the chemist, Emil Fischer where he carried out some early experiments on bile pigments.
He returned to Munich in 1911 and after one year, qualified as lecturer in internal medicine.
From 1913 to 1916 he served as a lecturer in physiology at the Physiological Institute in Munich.
In 1916 he succeeded Adolf Otto Reinhold Winaus as Professor of Medical Chemistry at the University of Innsbruck.
After two years, he was invited to hold the chair of Medical chemistry at the University of Vienna.
Hans Fischer’s most significant work is his synthesis of hemin, the crystalline product of hemoglobin. He split in half the molecule of bilirubin, a bile pigment related to hemin, and obtained a new acid that contained a section of the hemin molecule. Fischer recognized its structure and found that it was related to pyrrole. In this way, he performed the artificial synthesis of hemin from the structure of simpler compounds.