IP Library Granted Patent US 11,384,172
Granted Patent B2
US 11,384,172 · App. 16/061,809 · Granted Jul 12, 2022

Polymer, antimicrobial agent, disinfectant, antimicrobial material, disinfectant material, antimicrobial method, and disinfecting method

Inventors: Hidenori Naruse (Minato-ku, JP); Atsushi Itou (Minato-ku, JP); Shigeru Ikawa (Minato-ku, JP); Tsutomu Shimokawa (Minato-ku, JP); Masato Suzuki (Shinjuku-ku, JP); Mari Matsui (Shinjuku-ku, JP); Satowa Suzuki (Shinjuku-ku, JP); Keigo Shibayama (Shinjuku-ku, JP); Kazuhiro Ikkyuu (Minato-ku, JP)
Assignees: JSR CORPORATION; JAPAN AS REPRESENTED BY DIRECTOR-GENERAL OF NATIONAL INSTITUTE of INFECTIOUS DISEASES; JSR LIFE SCIENCES CORPORATION
C08F8/30A01N25/10A01N25/34A01N33/12C08F8/02C08F8/32C08F8/44C08F20/34C08F20/70C08F220/34C08F222/22C08G81/024C08L5/00C08L25/06C08L67/04C08F4/48C08F2800/20C08F2810/40C08G73/02C08L79/02C08L2203/02
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Quick Facts
Patent No.
US 11,384,172
App. No.
16/061,809
Granted
Jul 12, 2022
Kind
B2
Abstract

Provided is a polymer having antimicrobial and disinfecting properties against a wide range of kinds of germs. A polymer, including: a polymer chain having a repeating unit represented by the following formula (1); and a partial structure (excluding the polymer chain) derived from a compound containing a group represented by —NH—. [In formula (1), R 1 represents a hydrogen atom or a methyl group, Z represents a group forming an organic ammonium salt, —NR 5 R 6 (where R 5 and R 6 each independently represent a hydrogen atom, or a substituted or unsubstituted hydrocarbon group), or a substituted or unsubstituted nitrogen-containing heterocyclic group, and X represents a single bond, or a divalent linking group.]

Claims (35)

1. A polymer, comprising:

a polymer chain ending with a terminal compound and bonded to the terminal compound with a —NH— group

present in the compound;

wherein the compound comprises a plurality of —NH— groups,

wherein the polymer chain comprises a repeating unit of formula (1) and a repeating unit of formula (2):

wherein

R 1 represents a hydrogen atom or a methyl group,

Z represents an organic ammonium salt or an organic ammonium salt and —NR 5 R 6 ,

wherein R 5 and R 6 each independently represent a hydrogen atom, or a substituted or unsubstituted hydrocarbon group,

the organic ammonium salt is selected from the group consisting of —N + R 2 R 3 R 4 Y y− , —(C═O)O − N + HR 2 R 3 R 4 , and —(C═O)O −− A + wherein R 2 to R 4 each independently represent a hydrogen atom, a substituted or unsubstituted hydrocarbon group, Y y− represents a y-valent counter anion, and A + represents a quaternary ammonium cation,

and

X represents a single bond, a methylene group, an alkylene group, —(C═O)OR 11 -(*), or —(C═O)NHR 12 -(*) wherein R 11 and R 12 each represent a methylene group, an alkylene group, or an alkylene oxyalkylene group, and “*” represents a chemical bond bonded to the Z;

wherein

R 7 represents a hydrogen atom or a methyl group, and

A represents an aromatic hydrocarbon group, —(C═O)OR 8 , —(C═O)NHR 9 , or —OR 10 , wherein R 8 to R 10 each represent a hydrocarbon group or a group having a chain ether structure or a cyclic ether structure.

2. The polymer according to claim 1 ,

wherein a weight average molecular weight (Mw) of the polymer chain is 3,000 or less in terms of polystyrene measured by gel permeation chromatography, wherein a mobile phase is tetrahydrofuran.

3. The polymer according to claim 1 ,

wherein

Z is an organic ammonium salt of formula —N + R 2 R 3 R 4 Y y− , wherein R 2 to R 4 each independently represent a hydrogen atom, or a substituted or unsubstituted hydrocarbon group, and Y y− represents a y-valet counter anion, or

Z is an organic ammonium salt of formula —N + R 2 R 3 R 4 Y y− and —NR 5 R 6 .

4. The polymer according to claim 1 ,

wherein X is —(C═O)OR 11 -(*), —(C═O)NHR 12 -(*), and

wherein R 11 and R 12 each represent a methylene group, an alkylene group, or an alkylene oxyalkylene group.

5. The polymer according to claim 1 ,

wherein the compound is a compound comprising at least one selected from the group consisting of a primary amino group, a secondary amino group, and a carbamoyl group.

6. The polymer according to claim 1 ,

wherein the compound is a polyaziridine-polymer, a modified polyaziridine polymer, a diamine compound, a biguanide compound, an amino acid, an N-acylamino acid, a peptide, an amino sugar, a polyamine sugar, or an antimicrobial drug.

7. The polymer according to claim 1 ,

wherein the terminal compound further comprises a divalent group formed by ring opening of a cyclic ether group bonded to a —NH— group which is different from the group bonded to the polymer chain end.

8. An antimicrobial agent, a disinfectant, or an antimicrobial and disinfecting agent, comprising the polymer according to claim 1 as an active component.

9. An antimicrobial material, a disinfectant material, or an antimicrobial and disinfecting material, comprising the polymer according to claim 1 .

10. An antimicrobial method, a disinfecting method, or an antimicrobial and disinfecting method, comprising

providing an antimicrobial and/or disinfecting property with the polymer according to claim 1 .

11. The polymer according to claim 1 , wherein a content of the repeating unit (1) wherein Z is an organic ammonium salt is 60% by mole or more.

Assignments (5)
CHANGE OF NAME Recorded Mar 25, 2026
From: JSR LIFE SCIENCES CORPORATION
To: MBL MATERIALS CO., LTD.
Reel/Frame 075228/0228 →
CHANGE OF ADDRESS Recorded Mar 25, 2026
From: MBL MATERIALS CO., LTD.
To: MBL MATERIALS CO., LTD.
Reel/Frame 075228/0238 →
CHANGE OF NAME Recorded Sep 22, 2025
From: JICC-02 CORPORATION
To: JSR CORPORATION
Reel/Frame 072326/0282 →
MERGER Recorded Sep 22, 2025
From: JSR CORPORATION
To: JICC-02 CORPORATION
Reel/Frame 072935/0152 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2018
From: NARUSE, HIDENORI; ITOU, ATSUSHI; IKAWA, SHIGERU; SHIMOKAWA, TSUTOMU; SUZUKI, MASATO; MATSUI, MARI; SUZUKI, SATOWA; SHIBAYAMA, KEIGO; IKKYUU, KAZUHIRO
To: JSR CORPORATION; JAPAN AS REPRESENTED BY DIRECTOR-GENERAL OF NATIONAL INSTITUTE OF INFECTIOUS DISEASES; JSR LIFE SCIENCES CORPORATION
Reel/Frame 046072/0121 →
Priority Claims (1)
JP JP2015-242866 · Dec 14, 2015 · national
Continuity (1)
Related Publication 20180360033A1 · Dec 20, 2018
Cited By (1)
US 12,317,892