BE513091A - - Google Patents
Info
- Publication number
- BE513091A BE513091A BE513091DA BE513091A BE 513091 A BE513091 A BE 513091A BE 513091D A BE513091D A BE 513091DA BE 513091 A BE513091 A BE 513091A
- Authority
- BE
- Belgium
- Prior art keywords
- process according
- page
- formula
- lines
- salts
- Prior art date
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- XEKOWRVHYACXOJ-UHFFFAOYSA-N acetic acid ethyl ester Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 10
- 239000002904 solvent Substances 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 9
- 239000011780 sodium chloride Substances 0.000 claims description 9
- XZMCDFZZKTWFGF-UHFFFAOYSA-N carbodiimide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- 238000009835 boiling Methods 0.000 claims description 6
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 5
- 125000002091 cationic group Chemical group 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 239000003599 detergent Substances 0.000 claims description 5
- 238000007792 addition Methods 0.000 claims description 4
- 230000000844 anti-bacterial Effects 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 150000005215 alkyl ethers Chemical class 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- 230000000875 corresponding Effects 0.000 claims description 2
- 239000002798 polar solvent Substances 0.000 claims description 2
- 239000012429 reaction media Substances 0.000 claims description 2
- HWZGZWSHHNWSBP-UHFFFAOYSA-N 3-(2,3-diaminophenoxy)benzene-1,2-diamine Chemical class NC1=CC=CC(OC=2C(=C(N)C=CC=2)N)=C1N HWZGZWSHHNWSBP-UHFFFAOYSA-N 0.000 claims 1
- 230000003385 bacteriostatic Effects 0.000 claims 1
- 239000012458 free base Substances 0.000 claims 1
- 230000004927 fusion Effects 0.000 claims 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 235000019441 ethanol Nutrition 0.000 description 7
- 238000010992 reflux Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 238000000926 separation method Methods 0.000 description 6
- 238000002425 crystallisation Methods 0.000 description 5
- 230000005712 crystallization Effects 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000003610 charcoal Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 230000000622 irritating Effects 0.000 description 3
- -1 lauryl ether dichlorhydrate Chemical compound 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 description 2
- YOBWBLFILQYRFY-UHFFFAOYSA-M 2-hexadecylpyridine;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCC1=CC=CC=N1 YOBWBLFILQYRFY-UHFFFAOYSA-M 0.000 description 2
- MTNLEKFLKGGTKS-UHFFFAOYSA-N 4-(2,4-diaminophenoxy)benzene-1,3-diamine Chemical class NC1=CC(N)=CC=C1OC1=CC=C(N)C=C1N MTNLEKFLKGGTKS-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- JDAHCCZHQBMCDQ-UHFFFAOYSA-N 4-butoxybenzene-1,3-diamine;dihydrochloride Chemical compound Cl.Cl.CCCCOC1=CC=C(N)C=C1N JDAHCCZHQBMCDQ-UHFFFAOYSA-N 0.000 description 1
- ZYXPIHIXCMHBKI-UHFFFAOYSA-N 4-propoxybenzene-1,3-diamine;dihydrochloride Chemical compound Cl.Cl.CCCOC1=CC=C(N)C=C1N ZYXPIHIXCMHBKI-UHFFFAOYSA-N 0.000 description 1
- XIWMTQIUUWJNRP-UHFFFAOYSA-N Amidol Chemical compound NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 description 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N Dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
- 241001539176 Hime Species 0.000 description 1
- 210000004940 Nucleus Anatomy 0.000 description 1
- 230000001476 alcoholic Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000004429 atoms Chemical group 0.000 description 1
- 244000052616 bacterial pathogens Species 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000012295 chemical reaction liquid Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002349 favourable Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N nitric acid Chemical class O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 230000001376 precipitating Effects 0.000 description 1
- 230000002035 prolonged Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE513091A true BE513091A (ko) |
Family
ID=151317
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE513091D BE513091A (ko) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE513091A (ko) |
-
0
- BE BE513091D patent/BE513091A/fr unknown
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