Definition of Diamins

1. diamin [n] - See also: diamin

Lexicographical Neighbors of Diamins

diaminobenzidines
diaminocyclohexyl
diaminoethane
diaminoethanes
diaminofluorescein
diaminofluoresceins
diaminomonocarboxylic
diaminophenol
diaminophenols
diaminopimelate
diaminopimelates
diaminopimelic
diaminopimelic acid
diaminopropionate ammonia-lyase
diaminopyrimidine
diamins (current term)
diammoniate
diammoniates
diammonium
diamniotic
diamond
diamond-back
diamond-shaped murmur
diamond carries
diamond carry
diamond cross
diamond crossing
diamond crossings
diamond crossover
diamond cutter

Literary usage of Diamins

Below you will find example usage of this term as found in modern and/or classical literature:

1. A Manual of clinical diagnosis by means of microscopic and chemical methods by Charles Edmund Simon (1907)
"All attempts to isolate diamins from the urine under other pathological conditions at least have given rise to negative results. Regarding the origin of the ..."

2. The Medical student's manual of chemistry by Rudolph August Witthaus (1906)
"... contain a single amido group, and retain an alcoholic hydroxyl. In the diamins both ... diamins ..."

3. The American Journal of the Medical Sciences by Southern Society for Clinical Investigation (U.S.) (1902)
"An examination for diamins, or of the urine of the patient's family for cystin, ... An examination for diamins was not made. Of the remaining two cases Dr. ..."

4. A Manual of Clinical Diagnosis by Means of Microscopical and Chemical by Charles Edmund Simon (1904)
"Upon standing for from twelve to forty-eight hours the benzoylated diamins separate out in the milky fluid in the form of a more or less voluminous sediment ..."

5. A Reference handbook of the medical sciences embracing the entire range of by Albert Henry Buck (1908)
"These diamins, moreover, could be found as well in the ... Since, as Brieger showed, the diamins develop only in certain definite putrefactive processes, ..."

6. Chemical and microscopical diagnosis: By Francis Carter Wood by Francis Carter Wood (1905)
"The crystals obtained if both diamins are present, lose their water of crystallization when heated to 120° C., and melt at 140° C. Some of the benzoylated ..."

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