PL3757B1 - Method of securing wool, fur, etc. from moths - Google Patents
Method of securing wool, fur, etc. from moths Download PDFInfo
- Publication number
- PL3757B1 PL3757B1 PL3757A PL375724A PL3757B1 PL 3757 B1 PL3757 B1 PL 3757B1 PL 3757 A PL3757 A PL 3757A PL 375724 A PL375724 A PL 375724A PL 3757 B1 PL3757 B1 PL 3757B1
- Authority
- PL
- Poland
- Prior art keywords
- fur
- wool
- moths
- securing
- nitrogen
- Prior art date
Links
- 210000002268 wool Anatomy 0.000 title claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- YUDBKSANIWMLCU-UHFFFAOYSA-N 3,4-dichlorophthalic acid Chemical compound OC(=O)C1=CC=C(Cl)C(Cl)=C1C(O)=O YUDBKSANIWMLCU-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- ALIFPGGMJDWMJH-UHFFFAOYSA-N n-phenyldiazenylaniline Chemical compound C=1C=CC=CC=1NN=NC1=CC=CC=C1 ALIFPGGMJDWMJH-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 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
- -1 triphenyl guanidinium Chemical compound 0.000 description 1
Description
Spostrzezono, ze zwiazki chemiczne za- R wierajace grupe — N — X = Y mozna stosowac w charakterze srodka zapobie- £j gawczego przeciwko molom. We wzorze powyzszym X oznacza azot lub wegiel; Y — azot, wegiel lub pierscien, wreszcie R - wodór lub rodnik, jak np: metyl, etyl, fenyl, acetyl, benzoyl — CH2 — COOH i t d.CO CB* 1 r HN — N = C—H — pyrazolon Dla przykladu przytacza sie: H Q C2H5 —O. CO . C6//4 - N — N = CH. CH3 — hydrazon estru etylowego kwasu etylidenofenylokarbonowego N co.cns H CeH, — N — C = N — I NH.QHS — acetylodwu- chlorodwufe- nyloimid CRH,- JQ11Ó trójfe- nylo- guani- dynaw ci c\ :¦. I i co — c — c — co I II I N02 — CsHt - N — N = C C = N — N — C^.NO.I I.C//3 CHS I HOtS — C%H%, — N — N = CH. C6HZ — fcenzylkleaofenyloinetylohyclrazon kwasu sulfonowego.H C6HZ — N — N = N. C6U5 dwuazoaminobenzol, H CO I / \ C6//6 — N — N C6H2. Cl2 fcnylohydrazyd kwasu dwuchloroftalowego.\ / CO chlorek bais - nitrofenyloniezylopyraizoilonu.Ciala te nalezy uwiazac jedynie, jako przyklad rozmaitego ukladu wewmaftrz sa¬ mej grupy czynnej; zaleznie od warunków mozna dobierac badz resizty batrdiziej alifa¬ tycznej, wskutek czeigo ciala te wogóle wy¬ kazuja wieksiza rozpusizczailnose w rozpu¬ szczalnikach organicznych, (badz grupy o wiekszym a^ezanze czasteczkowym z lancu¬ chami otwartemi lub pierscieniowiemiif nie¬ kiedy zawieraljape grupe chlorowioowa, kar¬ boksylowa, sul|onow(a i i. d. Grupe czynna mozna, rozumie sie, w czasteczce uwielo1- krotnic.Dla zabezpieczenia od moli wyrobów weliniainych, futrzanych i t, p- wystarczy je pokryc w jakikolwiek sposób chocby jak najmniejsza iloscia zwiazków, o których mowanp. mozna welne skropic rozpuszczo¬ nym w benzolu powyzszym zwiazkiem lub tez zanurzyc ja na jakis czas w tym roz¬ tworze. PLIt has been found that chemical compounds containing the group - N - X = Y can be used as a narcotizing agent against moths. In the formula above, X is nitrogen or carbon; Y - nitrogen, carbon or ring, and finally R - hydrogen or a radical, such as: methyl, ethyl, phenyl, acetyl, benzoyl - CH2 - COOH and d. CO CB * 1 r HN - N = C — H - pyrazolone For example citation is: HQ C2H5 —O. WHAT . C6 // 4 - N - N = CH. CH3 - ethylidene phenyl carbonic acid ethyl ester hydrazone N co.cns H CeH, - N - C = N - I NH.QHS - acetyl di-chlorodibuhylimide CRH, - JQ11Ó triphenyl guanidinium c \: ¦. I i co - c - c - co I II I N02 - CsHt - N - N = CC = N - N - C ^ .NO.I IC // 3 CHS I HOtS - C% H%, - N - N = CH. C6HZ - fcenzylkleaophenylethylhydroclrazone of sulfonic acid. H C6HZ - N - N = N. C6U5 diazoaminobenzole, H CO I / \ C6 // 6 - N - N C6H2. Cl2 fcnylhydrazide of dichlorophthalic acid. / COchloride of bais - nitrophenylnonzylpyraizoylone. These bodies need only be included as an example of a different arrangement within the intrauterine group; depending on the conditions, it is possible to select aliphatic batrdi resistances, as a result of which these bodies generally exhibit greater dissolution in organic solvents (or groups with a greater molecular weight with open lances or chlorinated rings, and no group when , carboxylic, sulonow (ai and id The active group can, of course, be multiplied in a molecule. In order to protect vellum, fur and etc. products from moles, it is enough to cover them in any way with the least amount of compounds for which For example, wool can be sprinkled with the above compound dissolved in benzol, or it can be immersed in this solution for some time.
Claims (1)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL3757B1 true PL3757B1 (en) | 1926-02-27 |
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