DD142888A5 - Verfahren zur herstellung von phosphor-kohlenstoff-stickstoff-bindung enthaltenden verbindungen - Google Patents

Verfahren zur herstellung von phosphor-kohlenstoff-stickstoff-bindung enthaltenden verbindungen Download PDF

Info

Publication number: DD142888A5
Authority: DD; German Democratic Republic
Prior art keywords: water; phosphorus; acid; carbon; item
Prior art date: 1978-04-11

Application number

DD79212157A

Other languages

German (de)

English (en)

Inventor

Sandor Balint

Zoltan Kolonics

Antal Gaal

Jozsef Farkas

Laszlo Dufek

Sandor Horvath

Bela Karacsonyi

Original Assignee

Nitrokemia Ipartelepek

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.)

1978-04-11

Filing date

1979-04-11

Publication date

1980-07-16

1979-04-11 Application filed by Nitrokemia Ipartelepek filed Critical Nitrokemia Ipartelepek

1980-07-16 Publication of DD142888A5 publication Critical patent/DD142888A5/de

Links

150000001875 compounds Chemical class 0.000 title claims description 18
238000004519 manufacturing process Methods 0.000 title description 3
229910052757 nitrogen Inorganic materials 0.000 title 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 title 1
238000000034 method Methods 0.000 claims description 17
238000006243 chemical reaction Methods 0.000 claims description 16
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 9
239000002253 acid Substances 0.000 claims description 9
FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 claims description 8
150000003335 secondary amines Chemical class 0.000 claims description 7
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Natural products NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims description 6
150000001299 aldehydes Chemical class 0.000 claims description 6
HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims description 6
150000002576 ketones Chemical class 0.000 claims description 6
239000011541 reaction mixture Substances 0.000 claims description 6
239000004471 Glycine Substances 0.000 claims description 5
NMPVEAUIHMEAQP-UHFFFAOYSA-N 2-Bromoacetaldehyde Chemical compound BrCC=O NMPVEAUIHMEAQP-UHFFFAOYSA-N 0.000 claims description 4
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims description 4
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
229910021529 ammonia Inorganic materials 0.000 claims description 4
JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 claims description 4
229910052698 phosphorus Inorganic materials 0.000 claims description 4
239000011574 phosphorus Substances 0.000 claims description 4
-1 phosphorus halide Chemical class 0.000 claims description 4
150000003141 primary amines Chemical class 0.000 claims description 4
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 3
QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims description 3
HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 claims description 2
KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 2
IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 claims description 2
150000001412 amines Chemical class 0.000 claims description 2
150000003863 ammonium salts Chemical class 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
239000003960 organic solvent Substances 0.000 claims description 2
229920006395 saturated elastomer Polymers 0.000 claims description 2
BULLHNJGPPOUOX-UHFFFAOYSA-N chloroacetone Chemical compound CC(=O)CCl BULLHNJGPPOUOX-UHFFFAOYSA-N 0.000 claims 1
125000004430 oxygen atom Chemical group O* 0.000 claims 1
239000000047 product Substances 0.000 description 14
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 13
239000000203 mixture Substances 0.000 description 12
238000002360 preparation method Methods 0.000 description 12
238000009835 boiling Methods 0.000 description 9
238000003756 stirring Methods 0.000 description 7
238000000354 decomposition reaction Methods 0.000 description 6
238000010992 reflux Methods 0.000 description 6
239000000243 solution Substances 0.000 description 6
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 6
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 5
238000001816 cooling Methods 0.000 description 5
235000019441 ethanol Nutrition 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 4
239000003153 chemical reaction reagent Substances 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 4
230000002363 herbicidal effect Effects 0.000 description 4
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
239000006227 byproduct Substances 0.000 description 3
239000007795 chemical reaction product Substances 0.000 description 3
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
239000004480 active ingredient Substances 0.000 description 2
235000019270 ammonium chloride Nutrition 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
MOFCYHDQWIZKMY-UHFFFAOYSA-N chloromethylphosphonic acid Chemical compound OP(O)(=O)CCl MOFCYHDQWIZKMY-UHFFFAOYSA-N 0.000 description 2
239000013078 crystal Substances 0.000 description 2
150000005690 diesters Chemical class 0.000 description 2
230000000694 effects Effects 0.000 description 2
230000007062 hydrolysis Effects 0.000 description 2
238000006460 hydrolysis reaction Methods 0.000 description 2
238000002955 isolation Methods 0.000 description 2
238000002156 mixing Methods 0.000 description 2
FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 2
239000007858 starting material Substances 0.000 description 2
XDJWZONZDVNKDU-UHFFFAOYSA-N 1314-24-5 Chemical compound O=POP=O XDJWZONZDVNKDU-UHFFFAOYSA-N 0.000 description 1
HAAZMOAXEMIBAJ-UHFFFAOYSA-N 4-chloro-2-methylquinazoline Chemical compound C1=CC=CC2=NC(C)=NC(Cl)=C21 HAAZMOAXEMIBAJ-UHFFFAOYSA-N 0.000 description 1
USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
239000005695 Ammonium acetate Substances 0.000 description 1
ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
239000004254 Ammonium phosphate Substances 0.000 description 1
YNGIKVRSMOSWQG-UHFFFAOYSA-N C(#N)C1N(N(N(CC1)C)C#N)C#N Chemical compound C(#N)C1N(N(N(CC1)C)C#N)C#N YNGIKVRSMOSWQG-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical group OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
108010077895 Sarcosine Proteins 0.000 description 1
AKVPUSMVWHWDGW-UHFFFAOYSA-N [C].[N].[P] Chemical group [C].[N].[P] AKVPUSMVWHWDGW-UHFFFAOYSA-N 0.000 description 1
WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical compound CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
150000001414 amino alcohols Chemical class 0.000 description 1
229940043376 ammonium acetate Drugs 0.000 description 1
235000019257 ammonium acetate Nutrition 0.000 description 1
SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 1
239000001099 ammonium carbonate Substances 0.000 description 1
235000012501 ammonium carbonate Nutrition 0.000 description 1
235000011114 ammonium hydroxide Nutrition 0.000 description 1
229910000148 ammonium phosphate Inorganic materials 0.000 description 1
235000019289 ammonium phosphates Nutrition 0.000 description 1
ZRDJERPXCFOFCP-UHFFFAOYSA-N azane;iodic acid Chemical compound [NH4+].[O-]I(=O)=O ZRDJERPXCFOFCP-UHFFFAOYSA-N 0.000 description 1
PPBAJDRXASKAGH-UHFFFAOYSA-N azane;urea Chemical compound N.NC(N)=O PPBAJDRXASKAGH-UHFFFAOYSA-N 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000011109 contamination Methods 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
239000002178 crystalline material Substances 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
239000008098 formaldehyde solution Substances 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000012535 impurity Substances 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
VSAISIQCTGDGPU-UHFFFAOYSA-N phosphorus trioxide Inorganic materials O1P(O2)OP3OP1OP2O3 VSAISIQCTGDGPU-UHFFFAOYSA-N 0.000 description 1
230000001766 physiological effect Effects 0.000 description 1
239000001294 propane Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
229940043230 sarcosine Drugs 0.000 description 1
239000002689 soil Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
238000010189 synthetic method Methods 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl
- C07F9/3813—N-Phosphonomethylglycine; Salts or complexes thereof
- 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
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
General 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)
Luminescent Compositions (AREA)

DD79212157A 1978-04-11 1979-04-11 Verfahren zur herstellung von phosphor-kohlenstoff-stickstoff-bindung enthaltenden verbindungen DD142888A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
HU78NI213A HU177486B (en)	1978-04-11	1978-04-11	Process for preparing phosphonic acid derivatives

Publications (1)

Publication Number	Publication Date
DD142888A5 true DD142888A5 (de)	1980-07-16

Family

ID=11000006

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79212157A DD142888A5 (de)	1978-04-11	1979-04-11	Verfahren zur herstellung von phosphor-kohlenstoff-stickstoff-bindung enthaltenden verbindungen

Country Status (30)

Country	Link
JP (1)	JPS554362A (da)
AR (1)	AR227625A1 (da)
AT (1)	AT373602B (da)
BE (1)	BE875501A (da)
BG (1)	BG34334A3 (da)
BR (1)	BR7900568A (da)
CA (1)	CA1135279A (da)
CH (1)	CH642666A5 (da)
CS (1)	CS239903B2 (da)
DD (1)	DD142888A5 (da)
DE (1)	DE2914294C2 (da)
DK (1)	DK149473C (da)
EG (1)	EG13622A (da)
ES (1)	ES471960A1 (da)
FR (1)	FR2422675B1 (da)
GB (1)	GB2021589B (da)
GR (1)	GR67713B (da)
HU (1)	HU177486B (da)
IL (1)	IL57008A0 (da)
IN (1)	IN149779B (da)
IT (1)	IT1118553B (da)
LU (1)	LU81126A1 (da)
NL (1)	NL7902854A (da)
NO (1)	NO160373C (da)
PL (1)	PL123998B1 (da)
PT (1)	PT69461A (da)
RO (1)	RO78631A (da)
SU (1)	SU776561A3 (da)
TR (1)	TR20811A (da)
YU (1)	YU41154B (da)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IL72142A0 (en) *	1983-08-17	1984-10-31	Stauffer Chemical Co	Preparation of phosphonomethylated amino acids
GB2154588B (en) *	1984-02-20	1987-10-07	Sunlead Chemical Industry Co L	A process for preparation of n-phosphonomethyl glycine
JPS6134834U (ja) *	1985-07-24	1986-03-03	三菱農機株式会社	施肥装置付乗用水田作業機における肥料タンク等の取付装置
HU205944B (en) *	1988-02-08	1992-07-28	Nitrokemia Ipartelepek	Process for producing n-phosphono-methyl-imino-diacetic acid
GB8825589D0 (en) *	1988-11-02	1988-12-07	Albright & Wilson	Purification
HU203360B (en) *	1988-11-25	1991-07-29	Monsanto Co	Process for producing n-acylamino methylphosphonates
JP2525977B2 (ja) *	1991-10-17	1996-08-21	昭和電工株式会社	Ｎ−アシルアミノメチルホスホン酸の製造法
US5495042A (en) *	1993-11-04	1996-02-27	Cytogen Corporation	Non-alkaline purification of aminophosphonic acids
DE50200809D1 (de)	2001-01-12	2004-09-16	Basf Ag	Verfahren zur herstellung von n-phosphonomethyliminodiessigsäure
CN100400543C (zh) *	2006-09-08	2008-07-09	四川贝尔实业有限责任公司	亚氨基二乙腈水解制备双甘膦的方法

1978
- 1978-04-11 HU HU78NI213A patent/HU177486B/hu not_active IP Right Cessation
- 1978-07-21 ES ES471960A patent/ES471960A1/es not_active Expired
- 1978-08-03 SU SU782643651A patent/SU776561A3/ru active
1979
- 1979-01-30 BR BR7900568A patent/BR7900568A/pt unknown
- 1979-03-30 CH CH296679A patent/CH642666A5/de not_active IP Right Cessation
- 1979-04-03 GR GR58770A patent/GR67713B/el unknown
- 1979-04-03 IN IN332/CAL/79A patent/IN149779B/en unknown
- 1979-04-03 FR FR7908315A patent/FR2422675B1/fr not_active Expired
- 1979-04-03 GB GB7911510A patent/GB2021589B/en not_active Expired
- 1979-04-05 IL IL57008A patent/IL57008A0/xx unknown
- 1979-04-06 CS CS792378A patent/CS239903B2/cs unknown
- 1979-04-06 LU LU81126A patent/LU81126A1/xx unknown
- 1979-04-07 EG EG208/79A patent/EG13622A/xx active
- 1979-04-09 AT AT0263179A patent/AT373602B/de not_active IP Right Cessation
- 1979-04-09 RO RO7997178A patent/RO78631A/ro unknown
- 1979-04-09 DE DE2914294A patent/DE2914294C2/de not_active Expired
- 1979-04-10 BG BG043195A patent/BG34334A3/xx unknown
- 1979-04-10 PT PT69461A patent/PT69461A/pt unknown
- 1979-04-10 NO NO791217A patent/NO160373C/no unknown
- 1979-04-10 YU YU850/79A patent/YU41154B/xx unknown
- 1979-04-10 PL PL1979214793A patent/PL123998B1/pl unknown
- 1979-04-10 TR TR20811A patent/TR20811A/xx unknown
- 1979-04-10 DK DK148679A patent/DK149473C/da not_active IP Right Cessation
- 1979-04-11 CA CA000325294A patent/CA1135279A/en not_active Expired
- 1979-04-11 JP JP4409879A patent/JPS554362A/ja active Pending
- 1979-04-11 BE BE0/194546A patent/BE875501A/xx not_active IP Right Cessation
- 1979-04-11 NL NL7902854A patent/NL7902854A/xx not_active Application Discontinuation
- 1979-04-11 DD DD79212157A patent/DD142888A5/de not_active IP Right Cessation
- 1979-04-11 IT IT67767/79A patent/IT1118553B/it active
- 1979-04-11 AR AR276155A patent/AR227625A1/es active

Also Published As

Publication number	Publication date
CS239903B2 (en)	1986-01-16
DE2914294A1 (de)	1979-10-25
ATA263179A (de)	1983-06-15
JPS554362A (en)	1980-01-12
NO791217L (no)	1979-10-12
IT7967767A0 (it)	1979-04-11
IT1118553B (it)	1986-03-03
GR67713B (da)	1981-09-14
DK148679A (da)	1979-10-12
HU177486B (en)	1981-10-28
PL123998B1 (en)	1982-12-31
NO160373C (no)	1989-04-12
SU776561A3 (ru)	1980-10-30
GB2021589A (en)	1979-12-05
BE875501A (fr)	1979-07-31
PT69461A (en)	1979-05-01
CH642666A5 (de)	1984-04-30
BR7900568A (pt)	1979-10-30
DE2914294C2 (de)	1983-03-17
GB2021589B (en)	1982-10-20
RO78631A (ro)	1982-03-24
DK149473C (da)	1986-12-01
DK149473B (da)	1986-06-23
PL214793A1 (da)	1980-01-02
ES471960A1 (es)	1979-02-01
YU85079A (en)	1982-10-31
LU81126A1 (fr)	1979-07-20
FR2422675B1 (fr)	1986-03-21
IN149779B (da)	1982-04-10
BG34334A3 (en)	1983-08-15
IL57008A0 (en)	1979-07-25
EG13622A (en)	1982-03-31
AT373602B (de)	1984-02-10
CA1135279A (en)	1982-11-09
NL7902854A (nl)	1979-10-15
NO160373B (no)	1989-01-02
TR20811A (tr)	1982-09-15
FR2422675A1 (fr)	1979-11-09
YU41154B (en)	1986-12-31
AR227625A1 (es)	1982-11-30

Legal Events

Date	Code	Title	Description
1996-03-14	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DE1214229B (de)	1966-04-14	Verfahren zur Herstellung von Aminoalkylenphosphonsaeuren
CH646180A5 (de)	1984-11-15	Verfahren zur herstellung von n-phosphonomethyl-glycin.
EP0055695A1 (de)	1982-07-07	Verfahren zur Herstellung von N-phosphonomethylglycin
DD142888A5 (de)	1980-07-16	Verfahren zur herstellung von phosphor-kohlenstoff-stickstoff-bindung enthaltenden verbindungen
DE1938513B1 (de)	1970-12-23	Verfahren zur Herstellung von D-threo-1-p-Methylsulfonyl-phenyl-2-dichloracetamido-propan-1,3-diol
DE1248654B (de)	1967-08-31	Verfahren zur Herstellung von Phosphonsäuren und deren Salzen
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