𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Colorimetric estimation of ethanolamine with p-benzoquinone in the nanomole range

✍ Scribed by Annick Le Dur; Richard Chaby; Ladislas Szabó


Publisher
Elsevier Science
Year
1978
Tongue
English
Weight
462 KB
Volume
88
Category
Article
ISSN
0003-2697

No coin nor oath required. For personal study only.

✦ Synopsis


Ethanolamine reacts with p-benzoquinone in alkaline medium to give a product of undetermined structure, the absorption of which at 348 nm can be used for the estimation of the base. Conditions are described in which the interference of 0-phosphorylethanolamine, glucosamine, and neutral sugars is eliminated. The method was used to estimate the ethanolamine content of phospholipids alone and admixed to interfering substances. It is unreliable in the presence of amino acids or proteins.


📜 SIMILAR VOLUMES


Assay of reducing sugars in the nanomole
✍ Sabine Waffenschmidt; Lothar Jaenicke 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 285 KB

The photometric assay of reducing sugars with 2,2'-bicinchoninate was improved and its conditions were optimized. Optical density is linear between 1 and 25 nmol sugar/sample, and the assay is not affected by borate, phosphate, or other buffer anions. The molar extinction coefficients produced by th

Depression of iron uptake into erythrocy
✍ Robert L. Guy; Peidi Hu; Gisela Witz; Bernard D. Goldstein; Robert Snydert 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 357 KB

Using radio-iron uptake into erythrocytes as a measure of hematopoiesis, it was demonstrated that p benzoquinone (BQ) and muconaldehyde (MUC) are potent inhibitors of bone marrow function in female mice. These two benzene metabolites reduced iron uptake at dosages of <5-6 mg kg-'. The combination of

Unexpected formation of benzaldehydes by
✍ Kiyoshi Tanemura; Yoko Nishida; Tsuneo Suzuki; Koko Satsumabayashi; Takaaki Hora 📂 Article 📅 1997 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 263 KB

## Abstract 1,3‐Dithianes 1, 1,3‐dithiolanes 2, and diphenyl dithioacetals 3 derived from cinnamaldehydes reacted with 2,3‐dichloro‐5,6‐dicyano‐__p__‐benzoquinone in aqueous solvents to give benzaldehydes 4. Hydride transfer from 1–3 to 2,3‐dichloro‐5,6‐dicyano‐__p__‐benzoquinone followed by hydrol