ZA200603293B - Method of manufacture of polyacrolein - Google Patents

Method of manufacture of polyacrolein Download PDF

Info

Publication number: ZA200603293B
Authority: ZA; South Africa
Prior art keywords: polymer; acrolein; alcohol; solution; heating
Prior art date: 2003-11-06

Application number

ZA200603293A

Other languages

English (en)

Inventor

Tilbrook Matthew

Original Assignee

Chemeq Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2003-11-06

Filing date

2004-11-05

Publication date

2007-09-26

2003-11-06 Priority claimed from AU2003906117A external-priority patent/AU2003906117A0/en

2004-11-05 Application filed by Chemeq Ltd filed Critical Chemeq Ltd

2007-09-26 Publication of ZA200603293B publication Critical patent/ZA200603293B/en

Links

238000000034 method Methods 0.000 title claims abstract description 44
238000004519 manufacturing process Methods 0.000 title claims abstract description 8
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 claims abstract description 101
229920000642 polymer Polymers 0.000 claims abstract description 79
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 48
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 47
238000010438 heat treatment Methods 0.000 claims abstract description 26
229920005862 polyol Polymers 0.000 claims abstract description 8
150000003077 polyols Chemical class 0.000 claims abstract description 8
238000002156 mixing Methods 0.000 claims abstract description 5
239000000203 mixture Substances 0.000 claims description 58
239000002585 base Substances 0.000 claims description 26
239000007787 solid Substances 0.000 claims description 22
241000588724 Escherichia coli Species 0.000 claims description 14
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
239000002244 precipitate Substances 0.000 claims description 9
239000000178 monomer Substances 0.000 claims description 7
230000000845 anti-microbial effect Effects 0.000 claims description 6
241001465754 Metazoa Species 0.000 claims description 5
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 5
239000002253 acid Substances 0.000 claims description 5
230000003647 oxidation Effects 0.000 claims description 4
238000007254 oxidation reaction Methods 0.000 claims description 4
229920001515 polyalkylene glycol Polymers 0.000 claims description 4
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
229920001223 polyethylene glycol Polymers 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
238000013112 stability test Methods 0.000 claims description 3
238000003860 storage Methods 0.000 claims description 3
238000011282 treatment Methods 0.000 claims description 3
229910000288 alkali metal carbonate Inorganic materials 0.000 claims description 2
-1 alkali metal carbonate alkali metal hydroxide Chemical class 0.000 claims description 2
238000004090 dissolution Methods 0.000 claims description 2
239000003651 drinking water Substances 0.000 claims description 2
235000020188 drinking water Nutrition 0.000 claims description 2
235000013305 food Nutrition 0.000 claims description 2
230000002496 gastric effect Effects 0.000 claims description 2
208000015181 infectious disease Diseases 0.000 claims description 2
238000006116 polymerization reaction Methods 0.000 claims description 2
229910000027 potassium carbonate Inorganic materials 0.000 claims description 2
238000011321 prophylaxis Methods 0.000 claims description 2
239000002202 Polyethylene glycol Substances 0.000 claims 2
SGPGESCZOCHFCL-UHFFFAOYSA-N Tilisolol hydrochloride Chemical compound [Cl-].C1=CC=C2C(=O)N(C)C=C(OCC(O)C[NH2+]C(C)(C)C)C2=C1 SGPGESCZOCHFCL-UHFFFAOYSA-N 0.000 claims 2
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims 1
206010017964 Gastrointestinal infection Diseases 0.000 claims 1
239000004599 antimicrobial Substances 0.000 claims 1
150000001875 compounds Chemical class 0.000 claims 1
208000019836 digestive system infectious disease Diseases 0.000 claims 1
239000003814 drug Substances 0.000 claims 1
230000002906 microbiologic effect Effects 0.000 claims 1
230000002265 prevention Effects 0.000 claims 1
235000011182 sodium carbonates Nutrition 0.000 claims 1
239000000243 solution Substances 0.000 description 48
239000000523 sample Substances 0.000 description 35
229920000604 Polyethylene Glycol 200 Polymers 0.000 description 12
230000008569 process Effects 0.000 description 8
230000000694 effects Effects 0.000 description 5
239000011734 sodium Substances 0.000 description 5
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
239000003513 alkali Substances 0.000 description 3
239000012670 alkaline solution Substances 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
208000018522 Gastrointestinal disease Diseases 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
208000010643 digestive system disease Diseases 0.000 description 2
208000018685 gastrointestinal system disease Diseases 0.000 description 2
230000007774 longterm Effects 0.000 description 2
230000000813 microbial effect Effects 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
229910000029 sodium carbonate Inorganic materials 0.000 description 2
238000012360 testing method Methods 0.000 description 2
BIIBYWQGRFWQKM-JVVROLKMSA-N (2S)-N-[4-(cyclopropylamino)-3,4-dioxo-1-[(3S)-2-oxopyrrolidin-3-yl]butan-2-yl]-2-[[(E)-3-(2,4-dichlorophenyl)prop-2-enoyl]amino]-4,4-dimethylpentanamide Chemical compound CC(C)(C)C[C@@H](C(NC(C[C@H](CCN1)C1=O)C(C(NC1CC1)=O)=O)=O)NC(/C=C/C(C=CC(Cl)=C1)=C1Cl)=O BIIBYWQGRFWQKM-JVVROLKMSA-N 0.000 description 1
DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical class CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
QIGBRXMKCJKVMJ-UHFFFAOYSA-N 1,4-Benzenediol Natural products OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
241001397173 Kali <angiosperm> Species 0.000 description 1
AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 1
101000870345 Vasconcellea cundinamarcensis Cysteine proteinase 1 Proteins 0.000 description 1
150000008041 alkali metal carbonates Chemical class 0.000 description 1
230000002421 anti-septic effect Effects 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000003139 biocide Substances 0.000 description 1
210000000988 bone and bone Anatomy 0.000 description 1
125000002843 carboxylic acid group Chemical group 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000000645 desinfectant Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000003517 fume Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
239000003999 initiator Substances 0.000 description 1
235000013372 meat Nutrition 0.000 description 1
PSGAAPLEWMOORI-PEINSRQWSA-N medroxyprogesterone acetate Chemical compound C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2CC[C@]2(C)[C@@](OC(C)=O)(C(C)=O)CC[C@H]21 PSGAAPLEWMOORI-PEINSRQWSA-N 0.000 description 1
229910000000 metal hydroxide Inorganic materials 0.000 description 1
150000004692 metal hydroxides Chemical class 0.000 description 1
MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
XULSCZPZVQIMFM-IPZQJPLYSA-N odevixibat Chemical compound C12=CC(SC)=C(OCC(=O)N[C@@H](C(=O)N[C@@H](CC)C(O)=O)C=3C=CC(O)=CC=3)C=C2S(=O)(=O)NC(CCCC)(CCCC)CN1C1=CC=CC=C1 XULSCZPZVQIMFM-IPZQJPLYSA-N 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
RBWSWDPRDBEWCR-RKJRWTFHSA-N sodium;(2r)-2-[(2r)-3,4-dihydroxy-5-oxo-2h-furan-2-yl]-2-hydroxyethanolate Chemical compound [Na+].[O-]C[C@@H](O)[C@H]1OC(=O)C(O)=C1O RBWSWDPRDBEWCR-RKJRWTFHSA-N 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
239000006188 syrup Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N61/00—Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aliphatically bound aldehyde or keto groups, or thio analogues thereof; Derivatives thereof, e.g. acetals
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/74—Synthetic polymeric materials
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/74—Synthetic polymeric materials
- A61K31/765—Polymers containing oxygen
- A61K31/78—Polymers containing oxygen of acrylic acid or derivatives thereof
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F16/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F16/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F16/34—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an aldehydo radical
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
General Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Animal Behavior & Ethology (AREA)
Pharmacology & Pharmacy (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Polymers & Plastics (AREA)
Wood Science & Technology (AREA)
Dentistry (AREA)
Epidemiology (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Oncology (AREA)
Communicable Diseases (AREA)
General Chemical & Material Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Medicinal Preparation (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Compounds Of Unknown Constitution (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Polyethers (AREA)
Compositions Of Macromolecular Compounds (AREA)

ZA200603293A 2003-11-06 2004-11-05 Method of manufacture of polyacrolein ZA200603293B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
AU2003906117A AU2003906117A0 (en)		2003-11-06	Method of Manufacture of Polyacrolein

Publications (1)

Publication Number	Publication Date
ZA200603293B true ZA200603293B (en)	2007-09-26

Family

ID=34558179

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200603293A ZA200603293B (en)	2003-11-06	2004-11-05	Method of manufacture of polyacrolein

Country Status (14)

Country	Link
US (1)	US7767766B2 (fr)
EP (1)	EP1689795B1 (fr)
JP (1)	JP4680926B2 (fr)
KR (1)	KR20070000410A (fr)
CN (1)	CN100526342C (fr)
AT (1)	ATE461226T1 (fr)
BR (1)	BRPI0416298A (fr)
DE (1)	DE602004026096D1 (fr)
DK (1)	DK1689795T3 (fr)
EA (1)	EA009674B1 (fr)
ES (1)	ES2339025T3 (fr)
NZ (1)	NZ546949A (fr)
WO (1)	WO2005044874A1 (fr)
ZA (1)	ZA200603293B (fr)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US20100266653A1 (en) *	2007-07-19	2010-10-21	Chemeq Ltd	Biocidal polyacrolein composition
CN101168589B (zh) *	2007-08-14	2010-07-14	徐友志	一种新型树脂的生产工艺
JP5623285B2 (ja) *	2007-11-07	2014-11-12	レッキプロプライアタリーリミテッド	抗菌性ポリマーおよびその組成物
FR2932804B1 (fr) *	2008-06-19	2010-07-30	Arkema France	Polymere d'acroleine derive de matiere premiere renouvelable, son procede d'obtention et ses utilisations
CN101338004B (zh)	2008-08-22	2011-05-18	青岛康地恩药业有限公司	一种杀菌聚合物及其制备方法
FR2956404B1 (fr)	2010-02-15	2012-03-16	Arkema France	Procede d'obtention de polymeres d'acroleine, polymeres et leurs utilisations
WO2012010923A1 (fr) *	2010-07-19	2012-01-26	Arkema France	Procédé de fabrication d'acroléine à partir de glycérol
US10466269B2 (en)	2013-02-19	2019-11-05	Calamp Corp.	Systems and methods for low latency 3-axis accelerometer calibration
ES2755474T3 (es)	2014-11-18	2020-04-22	Recce Pharmaceuticals Ltd	Copolímero y método para el tratamiento de infecciones bacterianas
US10214166B2 (en) *	2015-06-11	2019-02-26	Calamp Corp.	Systems and methods for impact detection with noise attenuation of a sensor signal
WO2017139849A1 (fr) *	2016-02-19	2017-08-24	Recce Limited	Agent antiviral et méthode de traitement d'une infection virale
US10055909B2 (en)	2016-07-08	2018-08-21	Calamp Corp.	Systems and methods for crash determination
US10395438B2 (en)	2016-08-19	2019-08-27	Calamp Corp.	Systems and methods for crash determination with noise filtering
US10219117B2 (en)	2016-10-12	2019-02-26	Calamp Corp.	Systems and methods for radio access interfaces
US10473750B2 (en)	2016-12-08	2019-11-12	Calamp Corp.	Systems and methods for tracking multiple collocated assets
US10599421B2 (en)	2017-07-14	2020-03-24	Calamp Corp.	Systems and methods for failsafe firmware upgrades
US20190141156A1 (en)	2017-11-06	2019-05-09	Calamp Corp.	Systems and Methods for Dynamic Telematics Messaging
WO2021151160A1 (fr) *	2020-01-31	2021-08-05	Recce Pharmaceuticals Ltd	Procédé de préparation d'un copolymère biologiquement actif

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Publication number	Priority date	Publication date	Assignee	Title
DE2527795C3 (de)	1975-06-21	1978-04-06	Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler, 6000 Frankfurt	Jodophor-Lösung (A)
DE3205487C1 (de) *	1982-02-16	1983-10-13	Degussa Ag, 6000 Frankfurt	Verwendung von Polykondensationsprodukten aus Acrolein und Formaldehyd als Biozide
FR2580281B1 (fr) *	1985-04-11	1987-09-18	Synthelabo	Derives du nitrofuranne, leur preparation et leur application en therapeutique
US4724142A (en) *	1986-08-06	1988-02-09	Drew Chemical Corporation	Synergistic microbiocidal compositions containing a mixture of a N-alkyl dimethylbenzylammonium halide and an acrolein/formaldehyde polycondensation product
PH23983A (en) *	1986-12-23	1990-02-09	Biopolymers Ltd	Biostatic and biocidal composition
US4847392A (en) *	1987-03-17	1989-07-11	Regents Of The University Of Minnesota	Oxygen-substituted allyl cations as dienophiles
US4724143A (en) *	1987-06-17	1988-02-09	Drew Chemical Corporation	Synergistic microbiocidal composition containing a mixture of a bicyclic polyoxymethyleneoxazolidine and an acroloin/formaldehyde polycondensation product
DE4404404A1 (de) *	1994-02-11	1995-08-17	Degussa	Acroleinpolymer
AUPN327695A0 (en)	1995-05-30	1995-06-22	Chemeq Pty. Limited	Chemotherapeutic compositions
ES2157025T3 (es)	1996-02-22	2001-08-01	Degussa	Copolimeros que liberan acroleina.
US6060571A (en) *	1996-02-22	2000-05-09	Degussa Aktiengesellschaft	Acrolein-releasing copolymers
DE19653305A1 (de) *	1996-12-20	1998-08-13	Degussa	Acrolein freisetzende Emulsionshomopolymerisate
EA003138B1 (ru)	1998-07-17	2003-02-27	Кемек Лимитид	Водная композиция на основе поли(2-пропеналь, 2-пропеновой кислоты), способ её получения и её применение (варианты)
BR0009423B1 (pt) *	2000-02-16	2010-10-19		processo para aperfeiçoar a atividade antimicrobiana de um polìmero derivado de monÈmero de acroleìna.

2004
- 2004-11-05 WO PCT/AU2004/001537 patent/WO2005044874A1/fr not_active Ceased
- 2004-11-05 JP JP2006538600A patent/JP4680926B2/ja not_active Expired - Fee Related
- 2004-11-05 KR KR1020067011074A patent/KR20070000410A/ko not_active Withdrawn
- 2004-11-05 DK DK04796986.0T patent/DK1689795T3/da active
- 2004-11-05 BR BRPI0416298-6A patent/BRPI0416298A/pt not_active IP Right Cessation
- 2004-11-05 DE DE602004026096T patent/DE602004026096D1/de not_active Expired - Lifetime
- 2004-11-05 US US10/577,389 patent/US7767766B2/en not_active Expired - Fee Related
- 2004-11-05 NZ NZ546949A patent/NZ546949A/en not_active IP Right Cessation
- 2004-11-05 ES ES04796986T patent/ES2339025T3/es not_active Expired - Lifetime
- 2004-11-05 AT AT04796986T patent/ATE461226T1/de active
- 2004-11-05 CN CNB2004800322832A patent/CN100526342C/zh not_active Expired - Fee Related
- 2004-11-05 ZA ZA200603293A patent/ZA200603293B/en unknown
- 2004-11-05 EP EP04796986A patent/EP1689795B1/fr not_active Expired - Lifetime
- 2004-11-05 EA EA200600922A patent/EA009674B1/ru not_active IP Right Cessation

Also Published As

Publication number	Publication date
EA200600922A1 (ru)	2006-08-25
JP4680926B2 (ja)	2011-05-11
NZ546949A (en)	2009-01-31
ES2339025T3 (es)	2010-05-14
BRPI0416298A (pt)	2007-01-23
US7767766B2 (en)	2010-08-03
EP1689795B1 (fr)	2010-03-17
EP1689795A1 (fr)	2006-08-16
ATE461226T1 (de)	2010-04-15
WO2005044874A1 (fr)	2005-05-19
CN1875039A (zh)	2006-12-06
KR20070000410A (ko)	2007-01-02
DE602004026096D1 (de)	2010-04-29
JP2007510051A (ja)	2007-04-19
EA009674B1 (ru)	2008-02-28
HK1092485A1 (en)	2007-02-09
CN100526342C (zh)	2009-08-12
EP1689795A4 (fr)	2008-03-05
US20070083031A1 (en)	2007-04-12
DK1689795T3 (da)	2010-06-28

Publication	Publication Date	Title
ZA200603293B (en)	2007-09-26	Method of manufacture of polyacrolein
US20190000909A1 (en)	2019-01-03	Inhibiting or inactivating the virulence of a live pathogen
CA1295611C (fr)	1992-02-11	Complexe d'association a base de pullulane et de polyethyleneglycol,leur preparation et leurs utilisations
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