BE543052A - - Google Patents
Info
- Publication number
- BE543052A BE543052A BE543052DA BE543052A BE 543052 A BE543052 A BE 543052A BE 543052D A BE543052D A BE 543052DA BE 543052 A BE543052 A BE 543052A
- Authority
- BE
- Belgium
- Prior art keywords
- oxy
- salts
- amine
- fatty
- salt
- Prior art date
Links
- 150000001412 amines Chemical class 0.000 claims description 38
- 239000002253 acid Substances 0.000 claims description 22
- 150000007513 acids Chemical class 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 11
- 235000012208 gluconic acid Nutrition 0.000 claims description 9
- 239000000243 solution Substances 0.000 claims description 9
- RGHNJXZEOKUKBD-SQOUGZDYSA-N Gluconic acid Natural products OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 claims description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 claims description 7
- 239000000174 gluconic acid Substances 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 235000010469 Glycine max Nutrition 0.000 claims description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 4
- 244000068988 Glycine max Species 0.000 claims description 3
- 239000003929 acidic solution Substances 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 125000005702 oxyalkylene group Chemical group 0.000 claims description 3
- 125000006353 oxyethylene group Chemical group 0.000 claims 3
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 2
- -1 oxy-propylene group Chemical group 0.000 claims 2
- 239000011260 aqueous acid Substances 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 230000001747 exhibiting effect Effects 0.000 claims 1
- 239000000047 product Substances 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 238000005554 pickling Methods 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical class [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical group NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001323 aldoses Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- FGDMJJQHQDFUCP-UHFFFAOYSA-M sodium;2-propan-2-ylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=CC2=C(S([O-])(=O)=O)C(C(C)C)=CC=C21 FGDMJJQHQDFUCP-UHFFFAOYSA-M 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE543052A true BE543052A (cg-RX-API-DMAC10.html) |
Family
ID=171512
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE543052D BE543052A (cg-RX-API-DMAC10.html) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE543052A (cg-RX-API-DMAC10.html) |
-
0
- BE BE543052D patent/BE543052A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0102118B2 (en) | Cosmetic composition | |
| FR2532324A1 (fr) | Compositions detergentes stabilisees contenant un enzyme | |
| FR2648316A1 (fr) | Compositions herbicides a base de n-phosphonomethylglycine et leur utilisation | |
| US5952290A (en) | Anionic gemini surfactants and methods for their preparation | |
| FR2550959A1 (fr) | Agents tensio-actifs alcooliques polyoxyalkyles, compositions detergentes et agents de rincage les contenant | |
| FR2547316A1 (fr) | Procede de degraissage en milieu aqueux des peaux brutes et des peaux en tripe a l'aide d'amines organiques ethoxylees | |
| BE543052A (cg-RX-API-DMAC10.html) | ||
| US3626559A (en) | Process of shaping metal surfaces and cleaning the same | |
| US2739980A (en) | Salts of oxyalkylated fatty amines | |
| EP0607319A1 (en) | USE OF A TRIETHANOLAMINE PRODUCT BLEND. | |
| BE620530A (cg-RX-API-DMAC10.html) | ||
| US5120469A (en) | Amine oxide composition and process | |
| BE560753A (cg-RX-API-DMAC10.html) | ||
| FR2556364A1 (fr) | Compositions detergentes liquides exemptes de phosphate | |
| JP2000313975A (ja) | アルミニウム・アルミニウム合金用変色防止剤 | |
| BE399435A (cg-RX-API-DMAC10.html) | ||
| FR2523150A1 (fr) | Agents tensio-actifs et procede de preparation de tels agents | |
| BE476699A (cg-RX-API-DMAC10.html) | ||
| BE456506A (cg-RX-API-DMAC10.html) | ||
| BE383469A (cg-RX-API-DMAC10.html) | ||
| BE442671A (cg-RX-API-DMAC10.html) | ||
| FR2466501A1 (fr) | Composition de savon liquide aqueux et son procede de preparation | |
| CS265929B1 (cs) | Vodorozpustné mazivo, zejména pro tvářeni kovů | |
| BE718088A (cg-RX-API-DMAC10.html) | ||
| FR2556013A1 (fr) | Procede de post-traitement de substrats cellulosiques teints ou imprimes |