Heinrich Caro (February 13, 1834 – September 11, 1910), was a German chemist.

Heinrich Caro
Heinrich Caro
Born(1834-02-13)February 13, 1834
Posen, Prussia, now Poznań, Poland
DiedSeptember 11, 1910(1910-09-11) (aged 76)
Alma materUniversity of Göttingen, (1888)
Known forErlenmeyer azlactone synthesis Invention of eosin cell stain
Scientific career
InstitutionsUniversity of Strasbourg, kaiserliche biologische Anstallt Dahlem
Caro's grave in Mannheim

Caro was of Sephardic Jewish origin[1] He started his study of chemistry at the Friedrich Wilhelms University and later chemistry and dyeing in Berlin at the Royal Trades Institute. On the initiative of Nicolaus Druckenmüller, he trained as a calico printer in Germany, worked at Troost's calico printing works in Mülheim and then worked at the chemical firm Roberts, Dale in Manchester. During this time he improved the analysis of madder lake. After he returned to Germany he conducted his military service in 1857 and 1858. He worked in the laboratory of Jacques Meyer the father of Viktor Meyer in Berlin. In 1858 he was able to return to Mühlheim where he was not able to conduct his work. He joined the chemical firm Roberts, Dale in Manchester which he knew from his former visit. During his time in England he improved the extraction of Mauveine from the residues of the synthesis and developed a synthesis for aniline red and other dyes. In 1861 Caro returned to Germany and stayed at the laboratory of Robert Bunsen until he joined the Chemische Fabrik Dyckerhoff Clemm & Co. This chemical company later became BASF.

Caro was responsible for indigo research at BASF and he and Adolf von Baeyer synthesised the first indigo dye in 1878.[2] Caro also patented the dye alizarin on behalf of BASF. He was the first to isolate acridine and "Caro's acid" (peroxymonosulfuric acid) is named after him.

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References

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  1. ^ The History of an Obsession: German Judeophobia and the Holocaust by Klaus P. Fischer 1998, p.95
  2. ^ H. Caro, Carl Liebermann, Carl Graebe (1870). "Ueber die Fabrikation künstlichen Alizarins". Berichte der Deutschen Chemischen Gesellschaft. 3 (1): 359–360. doi:10.1002/cber.187000301122.{{cite journal}}: CS1 maint: multiple names: authors list (link)

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