CH526263A - Insektizid - Google Patents

Insektizid

Info

Publication number: CH526263A
Authority: CH; Switzerland
Prior art keywords: sep; textiles; triazine; heated; lower alkyl
Prior art date: 1969-10-01

Application number

CH1441270A

Other languages

German (de)

English (en)

Inventor

Wolfram Dr Dietsche

Heinrich Dr Adolphi

Peter Dr Beutel

Karl-Heinz Dr Koenig

Original Assignee

Basf Ag

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.)

1969-10-01

Filing date

1970-09-29

Publication date

1972-08-15

1970-09-29 Application filed by Basf Ag filed Critical Basf Ag

1972-08-15 Publication of CH526263A publication Critical patent/CH526263A/de

Links

239000002917 insecticide Substances 0.000 title 1
150000001875 compounds Chemical class 0.000 claims description 45
238000000034 method Methods 0.000 claims description 43
239000004753 textile Substances 0.000 claims description 40
229920000642 polymer Polymers 0.000 claims description 37
239000000463 material Substances 0.000 claims description 26
239000003054 catalyst Substances 0.000 claims description 22
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 19
229910052757 nitrogen Inorganic materials 0.000 claims description 19
230000008569 process Effects 0.000 claims description 18
125000000217 alkyl group Chemical group 0.000 claims description 17
238000011084 recovery Methods 0.000 claims description 13
239000000835 fiber Substances 0.000 claims description 12
229910052739 hydrogen Inorganic materials 0.000 claims description 12
239000001257 hydrogen Substances 0.000 claims description 12
229920002678 cellulose Polymers 0.000 claims description 11
239000001913 cellulose Substances 0.000 claims description 11
238000007385 chemical modification Methods 0.000 claims description 11
230000003213 activating effect Effects 0.000 claims description 10
125000001424 substituent group Chemical group 0.000 claims description 9
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
239000004372 Polyvinyl alcohol Substances 0.000 claims description 4
229920002451 polyvinyl alcohol Polymers 0.000 claims description 4
229920003043 Cellulose fiber Polymers 0.000 claims description 3
239000007983 Tris buffer Substances 0.000 claims description 3
125000004122 cyclic group Chemical group 0.000 claims description 3
230000000051 modifying effect Effects 0.000 claims description 3
239000013638 trimer Substances 0.000 claims description 3
238000011160 research Methods 0.000 claims description 2
230000001419 dependent effect Effects 0.000 claims 3
XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims 2
WOGXHNJBKGZMHV-UHFFFAOYSA-N 2-methoxypropanamide Chemical compound COC(C)C(N)=O WOGXHNJBKGZMHV-UHFFFAOYSA-N 0.000 claims 2
SXQFCVDSOLSHOQ-UHFFFAOYSA-N lactamide Chemical compound CC(O)C(N)=O SXQFCVDSOLSHOQ-UHFFFAOYSA-N 0.000 claims 2
229940080818 propionamide Drugs 0.000 claims 2
238000006243 chemical reaction Methods 0.000 description 40
239000004744 fabric Substances 0.000 description 36
229920000742 Cotton Polymers 0.000 description 21
239000000376 reactant Substances 0.000 description 17
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
239000000243 solution Substances 0.000 description 11
239000007864 aqueous solution Substances 0.000 description 10
235000015497 potassium bicarbonate Nutrition 0.000 description 10
239000011736 potassium bicarbonate Substances 0.000 description 10
229910000028 potassium bicarbonate Inorganic materials 0.000 description 10
TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 10
150000003254 radicals Chemical class 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
JUDYDQQRKGOMHY-UHFFFAOYSA-N C=NC(C(C)(OC)OC)=O Chemical compound C=NC(C(C)(OC)OC)=O JUDYDQQRKGOMHY-UHFFFAOYSA-N 0.000 description 8
150000001408 amides Chemical class 0.000 description 8
150000002825 nitriles Chemical class 0.000 description 8
-1 fluoromethylene Chemical group 0.000 description 7
150000001336 alkenes Chemical class 0.000 description 6
238000004132 cross linking Methods 0.000 description 6
239000002904 solvent Substances 0.000 description 6
238000005406 washing Methods 0.000 description 6
229920000297 Rayon Polymers 0.000 description 5
230000001965 increasing effect Effects 0.000 description 5
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 5
238000006116 polymerization reaction Methods 0.000 description 5
239000002964 rayon Substances 0.000 description 5
230000004584 weight gain Effects 0.000 description 5
235000019786 weight gain Nutrition 0.000 description 5
IHISWDOXUYNHSH-UHFFFAOYSA-N 1,4-dinitrobutane-2,3-diol Chemical compound [O-][N+](=O)CC(O)C(O)C[N+]([O-])=O IHISWDOXUYNHSH-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
238000010521 absorption reaction Methods 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
230000003197 catalytic effect Effects 0.000 description 4
239000000975 dye Substances 0.000 description 4
238000005470 impregnation Methods 0.000 description 4
239000000178 monomer Substances 0.000 description 4
230000035484 reaction time Effects 0.000 description 4
239000006227 byproduct Substances 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
150000002431 hydrogen Chemical group 0.000 description 3
230000006872 improvement Effects 0.000 description 3
230000004048 modification Effects 0.000 description 3
238000012986 modification Methods 0.000 description 3
150000002894 organic compounds Chemical class 0.000 description 3
238000012545 processing Methods 0.000 description 3
239000000047 product Substances 0.000 description 3
230000037303 wrinkles Effects 0.000 description 3
JENXNRAVMNIBRY-UHFFFAOYSA-N 1-[3,5-bis(3-methoxypropanoyl)-1,3,5-triazinan-1-yl]-3-methoxypropan-1-one Chemical compound COCCC(=O)N1CN(C(=O)CCOC)CN(C(=O)CCOC)C1 JENXNRAVMNIBRY-UHFFFAOYSA-N 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 2
238000005299 abrasion Methods 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
230000008901 benefit Effects 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000007844 bleaching agent Substances 0.000 description 2
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
150000004649 carbonic acid derivatives Chemical class 0.000 description 2
239000003153 chemical reaction reagent Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000001035 drying Methods 0.000 description 2
125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 2
125000000524 functional group Chemical group 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
239000000203 mixture Substances 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
229920001184 polypeptide Polymers 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
102000004196 processed proteins & peptides Human genes 0.000 description 2
108090000765 processed proteins & peptides Proteins 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
238000009988 textile finishing Methods 0.000 description 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
LKLLNYWECKEQIB-UHFFFAOYSA-N 1,3,5-triazinane Chemical compound C1NCNCN1 LKLLNYWECKEQIB-UHFFFAOYSA-N 0.000 description 1
QBPPRVHXOZRESW-UHFFFAOYSA-N 1,4,7,10-tetraazacyclododecane Chemical group C1CNCCNCCNCCN1 QBPPRVHXOZRESW-UHFFFAOYSA-N 0.000 description 1
FYBFGAFWCBMEDG-UHFFFAOYSA-N 1-[3,5-di(prop-2-enoyl)-1,3,5-triazinan-1-yl]prop-2-en-1-one Chemical compound C=CC(=O)N1CN(C(=O)C=C)CN(C(=O)C=C)C1 FYBFGAFWCBMEDG-UHFFFAOYSA-N 0.000 description 1
BPXCLLWXDHBFRH-UHFFFAOYSA-N 3-methoxypropanamide Chemical compound COCCC(N)=O BPXCLLWXDHBFRH-UHFFFAOYSA-N 0.000 description 1
244000198134 Agave sisalana Species 0.000 description 1
101100065878 Caenorhabditis elegans sec-10 gene Proteins 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
240000000491 Corchorus aestuans Species 0.000 description 1
235000011777 Corchorus aestuans Nutrition 0.000 description 1
235000010862 Corchorus capsularis Nutrition 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
101100134925 Gallus gallus COR6 gene Proteins 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
239000005708 Sodium hypochlorite Substances 0.000 description 1
229920002978 Vinylon Polymers 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
230000002152 alkylating effect Effects 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
235000011114 ammonium hydroxide Nutrition 0.000 description 1
125000000732 arylene group Chemical group 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
238000004061 bleaching Methods 0.000 description 1
238000009835 boiling Methods 0.000 description 1
235000009120 camo Nutrition 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
235000005607 chanvre indien Nutrition 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
238000009833 condensation Methods 0.000 description 1
208000012839 conversion disease Diseases 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000003517 fume Substances 0.000 description 1
229920000578 graft copolymer Polymers 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
239000011487 hemp Substances 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
229920001600 hydrophobic polymer Polymers 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
230000001939 inductive effect Effects 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
WHQSYGRFZMUQGQ-UHFFFAOYSA-N n,n-dimethylformamide;hydrate Chemical compound O.CN(C)C=O WHQSYGRFZMUQGQ-UHFFFAOYSA-N 0.000 description 1
239000012457 nonaqueous media Substances 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
239000004848 polyfunctional curative Substances 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
235000011181 potassium carbonates Nutrition 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
239000000985 reactive dye Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000004627 regenerated cellulose Substances 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
238000007363 ring formation reaction Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
239000004307 sodium orthophenyl phenol Substances 0.000 description 1
239000002195 soluble material Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000010025 steaming Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
230000008961 swelling Effects 0.000 description 1
150000003573 thiols Chemical class 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
231100000167 toxic agent Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
238000005303 weighing Methods 0.000 description 1
210000002268 wool Anatomy 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having three nitrogen atoms as the only ring hetero atoms
- C07F9/6518—Five-membered rings

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Molecular Biology (AREA)
Agronomy & Crop Science (AREA)
Biochemistry (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

CH1441270A 1969-10-01 1970-09-29 Insektizid CH526263A (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19691949490 DE1949490A1 (de)	1969-10-01	1969-10-01	Phosphorsaeureester Materialien

Publications (1)

Publication Number	Publication Date
CH526263A true CH526263A (de)	1972-08-15

Family

ID=5747025

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1441270A CH526263A (de)	1969-10-01	1970-09-29	Insektizid

Country Status (9)

Country	Link
JP (1)	JPS4911071B1 (fr)
BE (1)	BE756952A (fr)
CH (1)	CH526263A (fr)
DE (1)	DE1949490A1 (fr)
FR (1)	FR2068216A5 (fr)
GB (1)	GB1315017A (fr)
IL (1)	IL35356A (fr)
NL (1)	NL7014464A (fr)
ZA (1)	ZA706675B (fr)

0
- BE BE756952D patent/BE756952A/fr unknown
1969
- 1969-10-01 DE DE19691949490 patent/DE1949490A1/de active Pending
1970
- 1970-09-25 FR FR7034864A patent/FR2068216A5/fr not_active Expired
- 1970-09-28 IL IL35356A patent/IL35356A/en unknown
- 1970-09-29 JP JP45084750A patent/JPS4911071B1/ja active Pending
- 1970-09-29 CH CH1441270A patent/CH526263A/de not_active IP Right Cessation
- 1970-09-30 ZA ZA706675*A patent/ZA706675B/xx unknown
- 1970-09-30 GB GB4641870A patent/GB1315017A/en not_active Expired
- 1970-10-01 NL NL7014464A patent/NL7014464A/xx unknown

Also Published As

Publication number	Publication date
ZA706675B (en)	1971-07-28
JPS4911071B1 (fr)	1974-03-14
BE756952A (fr)	1971-04-01
FR2068216A5 (fr)	1971-08-20
IL35356A0 (en)	1970-11-30
GB1315017A (en)	1973-04-26
IL35356A (en)	1974-11-29
DE1949490A1 (de)	1971-04-08
NL7014464A (fr)	1971-04-05

Legal Events

Date	Code	Title	Description
1979-06-15	PL	Patent ceased

Publication	Publication Date	Title
DE864986C (de)	1953-01-29	Praeparat und Verfahren zum Appretieren von Textilien
CH643280A5 (de)	1984-05-30	Wasser- und oelabstossendes mittel fuer textilien mit hoher bestaendigkeit gegen waschen und trockenreinigen.
DE2058317A1 (de)	1971-06-03	Harnstoffverbindungen und deren Verwendung als Textilhilfsmittel
DE2256234A1 (de)	1973-05-24	Kationische oberflaechenaktive verbindungen, verfahren zu ihrer herstellung und ihre verwendung fuer die behandlung von textilmaterialien
DE2536678A1 (de)	1976-03-04	Verfahren zur herstellung von amphoteren, waessrigen harzemulsionen
DE2546956A1 (de)	1976-05-20	Verfahren zur herstellung von geweben mit dauerformbestaendigkeit
EP0033115A2 (fr)	1981-08-05	Procédé pour le finissage de matériaux textiles
CH526263A (de)	1972-08-15	Insektizid
DE1493227A1 (de)	1969-02-13	Verfahren zur Herstellung modifizierter Cellulosepolymere
DE3029537A1 (de)	1981-02-26	Zusammensetzung und verfahren zur herstellung eines knitterfesten stoffes unter verwendung dieser zusammensetzung
EP0013388A2 (fr)	1980-07-23	Agent d'apprêt textile et procédé pour sa préparation ainsi que son utilisation
DE1795262A1 (de)	1972-04-06	Waschfeste oelabweisende Ausruestung von Textilien
EP0359039A2 (fr)	1990-03-21	Procédé d'apprêt infraissable de matériaux textiles
DE2520005A1 (de)	1975-12-04	Verfahren zur herstellung von harnstoff-formaldehyd-glyoxal-kondensationsprodukten
DE1000007C2 (de)	1957-06-19	Verfahren zum Veredeln von Textilgut
DE2114610A1 (de)	1972-10-05	Derivate mehrwertiger Alkohole
DE2312090A1 (de)	1974-09-12	Poly-dialkylphosphonoalkylcarbonate und ihre verwendung zur flammschutzausruestung von cellulosehaltigem textilgut
AT213834B (de)	1961-03-10	Verfahren zum Veredeln von Textilgeweben
DE2219460A1 (de)	1972-10-26	Harz aus Crotonylidendiharnstoff-Glyoxal-Formaldehyd-Aminoplastmaterialfür Permanentpreßstoff bzw. -tuch
AT217213B (de)	1961-09-11	Verfahren zur Herstellung von Polymeraddukten
DE1124465B (de)	1962-03-01	Verfahren zur Kunstharzausruestung textiler Gebilde
DE1793357A1 (de)	1972-02-03	Fluorierte organische Verbindungen
DE2104730A1 (de)	1971-10-14	Perfluoralkylalkylmonocarbonsaureester, Verfahren zu deren Herstellung und deren Verwendung
DE2709019A1 (de)	1977-09-08	Verfahren zur behandlung eines fasergegenstandes
DE2319449C3 (de)	1976-11-25	Verfahren und Vorrichtung zur Flammfestausrüstung von cellulosehaltigen Materialien