NO130943B - - Google Patents

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Info

Publication number: NO130943B
Authority: NO; Norway
Prior art keywords: setting device; pin; piece; sleeve; damping piston
Prior art date: 1970-02-06

Application number

NO43271A

Other languages

English (en)

Norwegian (no)

Other versions

NO130943C (fr

Inventor

A Foldes

G Delmar

Original Assignee

Delmar Chem

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.)

1970-02-06

Filing date

1971-02-05

Publication date

1974-12-02

1971-02-05 Application filed by Delmar Chem filed Critical Delmar Chem

1974-12-02 Publication of NO130943B publication Critical patent/NO130943B/no

1975-03-12 Publication of NO130943C publication Critical patent/NO130943C/no

Links

239000000463 material Substances 0.000 claims description 3
238000013016 damping Methods 0.000 claims 7
238000004873 anchoring Methods 0.000 claims 4
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 2
239000007789 gas Substances 0.000 claims 2
239000003380 propellant Substances 0.000 claims 2
238000004140 cleaning Methods 0.000 claims 1
238000002485 combustion reaction Methods 0.000 claims 1
239000004567 concrete Substances 0.000 claims 1
238000006073 displacement reaction Methods 0.000 claims 1
239000002360 explosive Substances 0.000 claims 1
238000010304 firing Methods 0.000 claims 1
229910052742 iron Inorganic materials 0.000 claims 1
230000035939 shock Effects 0.000 claims 1
239000004575 stone Substances 0.000 claims 1
TXCGAZHTZHNUAI-UHFFFAOYSA-N clofibric acid Chemical class OC(=O)C(C)(C)OC1=CC=C(Cl)C=C1 TXCGAZHTZHNUAI-UHFFFAOYSA-N 0.000 description 17
UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 17
-1 amine salts Chemical class 0.000 description 12
150000001875 compounds Chemical class 0.000 description 11
KNHUKKLJHYUCFP-UHFFFAOYSA-N clofibrate Chemical compound CCOC(=O)C(C)(C)OC1=CC=C(Cl)C=C1 KNHUKKLJHYUCFP-UHFFFAOYSA-N 0.000 description 10
229960001214 clofibrate Drugs 0.000 description 9
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical class NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 8
238000000034 method Methods 0.000 description 8
150000003839 salts Chemical class 0.000 description 8
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
241000700159 Rattus Species 0.000 description 5
239000003921 oil Substances 0.000 description 5
239000000843 powder Substances 0.000 description 5
241000699670 Mus sp. Species 0.000 description 4
238000009835 boiling Methods 0.000 description 4
HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 4
238000002329 infrared spectrum Methods 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
239000000203 mixture Substances 0.000 description 4
239000000047 product Substances 0.000 description 4
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000004985 diamines Chemical class 0.000 description 3
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical class NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000012429 reaction media Substances 0.000 description 3
210000002966 serum Anatomy 0.000 description 3
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
239000003814 drug Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
125000004494 ethyl ester group Chemical group 0.000 description 2
230000009965 odorless effect Effects 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
241000894007 species Species 0.000 description 2
230000002110 toxicologic effect Effects 0.000 description 2
231100000027 toxicology Toxicity 0.000 description 2
MDLKWDQMIZRIBY-UHFFFAOYSA-N 1-(dimethylamino)ethanol Chemical class CC(O)N(C)C MDLKWDQMIZRIBY-UHFFFAOYSA-N 0.000 description 1
201000001320 Atherosclerosis Diseases 0.000 description 1
208000024172 Cardiovascular disease Diseases 0.000 description 1
206010012735 Diarrhoea Diseases 0.000 description 1
208000018522 Gastrointestinal disease Diseases 0.000 description 1
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
241001494479 Pecora Species 0.000 description 1
241000906446 Theraps Species 0.000 description 1
231100000215 acute (single dose) toxicity testing Toxicity 0.000 description 1
230000001154 acute effect Effects 0.000 description 1
231100000460 acute oral toxicity Toxicity 0.000 description 1
231100000570 acute poisoning Toxicity 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
125000005263 alkylenediamine group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
230000037396 body weight Effects 0.000 description 1
238000009395 breeding Methods 0.000 description 1
230000001488 breeding effect Effects 0.000 description 1
HUIKLQYJFNQHCJ-UHFFFAOYSA-N butyl 2-(4-chlorophenoxy)-2-methylpropanoate Chemical compound CCCCOC(=O)C(C)(C)OC1=CC=C(Cl)C=C1 HUIKLQYJFNQHCJ-UHFFFAOYSA-N 0.000 description 1
239000002775 capsule Substances 0.000 description 1
235000012000 cholesterol Nutrition 0.000 description 1
238000007405 data analysis Methods 0.000 description 1
229960002887 deanol Drugs 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical class CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000001647 drug administration Methods 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
210000001035 gastrointestinal tract Anatomy 0.000 description 1
230000007794 irritation Effects 0.000 description 1
231100001231 less toxic Toxicity 0.000 description 1
UXIVINXAZVEIMC-UHFFFAOYSA-N methyl 2-(4-chlorophenoxy)-2-methylpropanoate Chemical compound COC(=O)C(C)(C)OC1=CC=C(Cl)C=C1 UXIVINXAZVEIMC-UHFFFAOYSA-N 0.000 description 1
210000004877 mucosa Anatomy 0.000 description 1
239000000825 pharmaceutical preparation 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
OWWSWMUOQSRTBU-UHFFFAOYSA-N propyl 2-(4-chlorophenoxy)-2-methylpropanoate Chemical compound CCCOC(=O)C(C)(C)OC1=CC=C(Cl)C=C1 OWWSWMUOQSRTBU-UHFFFAOYSA-N 0.000 description 1
KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical class NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
229940124597 therapeutic agent Drugs 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
- C07C59/68—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NO43271A 1970-02-06 1971-02-05 NO130943C (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US941770A	1970-02-06	1970-02-06

Publications (2)

Publication Number	Publication Date
NO130943B true NO130943B (fr)	1974-12-02
NO130943C NO130943C (fr)	1975-03-12

Family

ID=21737522

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO43271A NO130943C (fr)	1970-02-06	1971-02-05

Country Status (8)

Country	Link
JP (1)	JPS5118484B1 (fr)
CA (1)	CA957373A (fr)
CH (1)	CH540214A (fr)
DE (1)	DE2105418C3 (fr)
FR (1)	FR2081494B1 (fr)
GB (1)	GB1336632A (fr)
NO (1)	NO130943C (fr)
SE (1)	SE375756B (fr)

1971
- 1971-02-02 CH CH151271A patent/CH540214A/fr not_active IP Right Cessation
- 1971-02-05 FR FR7103963A patent/FR2081494B1/fr not_active Expired
- 1971-02-05 SE SE144671A patent/SE375756B/xx unknown
- 1971-02-05 NO NO43271A patent/NO130943C/no unknown
- 1971-02-05 DE DE19712105418 patent/DE2105418C3/de not_active Expired
- 1971-02-05 JP JP46004680A patent/JPS5118484B1/ja active Pending
- 1971-02-08 CA CA104,687A patent/CA957373A/en not_active Expired
- 1971-04-19 GB GB2119271A patent/GB1336632A/en not_active Expired

Also Published As

Publication number	Publication date
JPS5118484B1 (fr)	1976-06-10
NO130943C (fr)	1975-03-12
FR2081494A1 (fr)	1971-12-03
DE2105418C3 (de)	1975-11-27
FR2081494B1 (fr)	1975-04-18
DE2105418A1 (de)	1971-08-12
GB1336632A (en)	1973-11-07
SE375756B (fr)	1975-04-28
DE2105418B2 (de)	1975-04-24
CH540214A (fr)	1973-08-15
CA957373A (en)	1974-11-05

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