BRPI0708314A2

BRPI0708314A2 - compostos antimicrobianos

compostos antimicrobianos Download PDF

Info

Publication number: BRPI0708314A2
Authority: BR; Brazil
Prior art keywords: formula; hydroxy; phenyl; alkyl; substituted
Prior art date: 2006-02-28

Application number

BRPI0708314-9A

Other languages

English (en)

Portuguese (pt)

Inventor

Werner H Hoelzl

Andrea Preuss

Michele Gerster

Original Assignee

Ciba Holding Inc

Priority date

2006-02-28

Filing date

2007-02-19

Publication date

2011-05-24

2007-02-19 Application filed by Ciba Holding Inc filed Critical Ciba Holding Inc

2011-05-24 Publication of BRPI0708314A2 publication Critical patent/BRPI0708314A2/pt

Links

150000001875 compounds Chemical class 0.000 title abstract description 27
230000000845 anti-microbial effect Effects 0.000 title abstract description 4
-1 cationic siloxane Chemical class 0.000 claims abstract description 163
239000000417 fungicide Substances 0.000 claims abstract description 5
239000000203 mixture Substances 0.000 claims description 87
150000001768 cations Chemical class 0.000 claims description 50
239000000463 material Substances 0.000 claims description 39
150000003839 salts Chemical class 0.000 claims description 31
150000001450 anions Chemical class 0.000 claims description 28
125000000217 alkyl group Chemical group 0.000 claims description 25
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 15
125000004423 acyloxy group Chemical group 0.000 claims description 10
125000003118 aryl group Chemical group 0.000 claims description 10
125000000753 cycloalkyl group Chemical group 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 10
229910052739 hydrogen Inorganic materials 0.000 claims description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
230000007935 neutral effect Effects 0.000 claims description 8
125000003545 alkoxy group Chemical group 0.000 claims description 7
125000001589 carboacyl group Chemical group 0.000 claims description 7
229910052736 halogen Inorganic materials 0.000 claims description 6
150000002367 halogens Chemical class 0.000 claims description 6
230000000855 fungicidal effect Effects 0.000 claims description 5
125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
229910019142 PO4 Inorganic materials 0.000 claims description 4
125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 3
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 3
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239000010452 phosphate Substances 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
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