✦ LIBER ✦

Factors influencing the rate of formation of volatile N-nitrosamines during the nitrosation of spermidine

✍ Scribed by Hildrum, Kjell I.; Scanlan, Richard A.

Book ID: 125975590
Publisher: American Chemical Society
Year: 1977
Tongue: English
Weight: 363 KB
Volume: 25
Category: Article
ISSN: 0021-8561
DOI: 10.1021/jf60210a010

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Formation of volatile, hydroxylated, and

Formation of volatile, hydroxylated, and chlorinated N-nitrosamines during the nitrosation of spermidine 3-hydrochloride

✍ Hildrum, Kjell I.; Scanlan, Richard A.; Libbey, Leonard M. 📂 Article 📅 1977 🏛 American Chemical Society 🌐 English ⚖ 432 KB

Formation of bis(hydroxyalkyl)-N-nitrosa

Formation of bis(hydroxyalkyl)-N-nitrosamines as products of the nitrosation of spermidine

✍ Hotchkiss, Joseph H.; Scanlan, Richard A.; Libbey, Leonard M. 📂 Article 📅 1977 🏛 American Chemical Society 🌐 English ⚖ 698 KB

Identification of .gamma.-butenyl-(.beta

Identification of .gamma.-butenyl-(.beta.-propenyl)nitrosamine, the principal volatile nitrosamine formed in the nitrosation of spermidine or spermine

✍ Hildrum, Kjell I.; Scanlan, Richard A.; Libbey, Leonard M. 📂 Article 📅 1975 🏛 American Chemical Society 🌐 English ⚖ 442 KB

The preferential formation of volatile N

The preferential formation of volatile N-nitrosamines in the fat of fried bacon

✍ Donald S. Mottram; Ronald L. S. Patterson; Robert A. Edwards; Terry A. Gough 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 English ⚖ 341 KB

Survey of human milk for volatile N-nitr

Survey of human milk for volatile N-nitrosamines and the influence of diet on their formation

✍ Lakritz, L.; Pensabene, J.W. 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 355 KB

Rapid nitrosamine formation from a terti

Rapid nitrosamine formation from a tertiary amine: The nitrosation of 2-(N,N-Dimethylaminomethyl)pyrrole

✍ R.N. Loeppky; J.R. Outram; W. Tomasik; J.M. Faulconer 📂 Article 📅 1983 🏛 Elsevier Science 🌐 French ⚖ 267 KB

2-(N,N-Dimethylaminomethyl)pyrrole reacts instantaneously with nitrous acid at 25" to produce diemthylnitrosamine, maleimidemonooxine, formaldehyde and other products. The data implicate new mechanisms of tertiary amine nitrosation. N-Alkyl tertiary amines react very slowly at 25" with nitrous acid