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United States Patent 0 F: Sept. 19, 1964, 5,228/ 64 Dine, 5-Methyl-2,4,6-Trichlor Pyrimidine, 5-Methyl-2,4-Di
United States Patent 0 F: Sept. 19, 1964, 5,228/ 64 Dine, 5-Methyl-2,4,6-Trichlor Pyrimidine, 5-Methyl-2,4-Di
3,429,780
10 Claims
media.
The inhibitors may be used either singly or several of
the inhibitors may be added to the media in which the
fermentation proceeds.
30
chlorotetracycline.
A more speci?c object is to inhibit in an effective man
TABLE
Overall
Example
Inhibitor
pyrimidine.
2 _______ __ 5-methy1-2, 4, 6-
trichloro-pyrimidine.
3 _______ -_ 5-methyl-2,4-dich1oro-
pyrimidine.
4 _______ ._ 2, l-diehloro-pyrl-
examples.
midine.
5 _______ -_ 2, 6-dichloro-7-methyl-
purine.
6_ _ _ .
. _- 2, 4-dieh1or0-pyrimidine
(2 meg/1111.).
triehloropyrimidine
(2 mcg./ml.).
7 ....... __ 5-methyl-2,4, 6-
3, 910
95
0. 4
3, 820
85
__________ _.
3,760
95
04
3, 660
80
__________ _.
3, 690
95
0. 4
3, 780
so
.......... ..
3, 810
95
3, 910
80
4
.......... .-
3, 640
80
0. 4
3, 520
75
__________ _.
3, 820
95
0 4
3, 760
85
.......... _.
4, 100
40
hibitor.
3,429,780
general formula
general formula
.2
/C\ C-X
N/
(ll-([3 \ /gb-Y
general formula
40
60 to inhibit chlorination.
3,429,780
References Cited
UNITED STATES PATENTS
3,019,173
1/1962
FOREIGN PATENTS
1,074,826
2/ 1960 Germany.
1951l4