DE85929C - - Google Patents
Info
- Publication number
- DE85929C DE85929C DENDAT85929D DE85929DA DE85929C DE 85929 C DE85929 C DE 85929C DE NDAT85929 D DENDAT85929 D DE NDAT85929D DE 85929D A DE85929D A DE 85929DA DE 85929 C DE85929 C DE 85929C
- Authority
- DE
- Germany
- Prior art keywords
- iodine
- compounds
- acid
- chlorinated
- salts
- Prior art date
- Legal status (The legal status 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 status listed.)
- Active
Links
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 20
- 239000011630 iodine Substances 0.000 claims description 14
- 229910052740 iodine Inorganic materials 0.000 claims description 14
- FYEHYMARPSSOBO-UHFFFAOYSA-N Aurin Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)=C1C=CC(=O)C=C1 FYEHYMARPSSOBO-UHFFFAOYSA-N 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 10
- 150000002497 iodine compounds Chemical class 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 150000007513 acids Chemical class 0.000 claims description 6
- 150000002496 iodine Chemical class 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 4
- 239000012670 alkaline solution Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- -1 iodine, chlorinated iodine, chlorinated iodine Chemical class 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 2
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000004571 lime Substances 0.000 claims description 2
- 239000002244 precipitate Substances 0.000 claims description 2
- GWEIHUNYMRRZJJ-MOAWTDCJSA-N Auricolic acid Chemical compound CC\C=C/CCC(O)C\C=C/CCCCCCCCCC(O)=O GWEIHUNYMRRZJJ-MOAWTDCJSA-N 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 20
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 235000011121 sodium hydroxide Nutrition 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 230000001376 precipitating effect Effects 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- SVTUIUDFRXDTID-UHFFFAOYSA-N OC(C=CC=C1I)=C1I.I Chemical compound OC(C=CC=C1I)=C1I.I SVTUIUDFRXDTID-UHFFFAOYSA-N 0.000 description 2
- ZVAKTWSQIIRIIH-UHFFFAOYSA-N [K].[I] Chemical compound [K].[I] ZVAKTWSQIIRIIH-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- VAPDZNUFNKUROY-UHFFFAOYSA-N 2,4,6-triiodophenol Chemical compound OC1=C(I)C=C(I)C=C1I VAPDZNUFNKUROY-UHFFFAOYSA-N 0.000 description 1
- AKMSPOLFRMQWSM-UHFFFAOYSA-N CC(C)C(C=CC(C)=C1I)=C1O.I Chemical compound CC(C)C(C=CC(C)=C1I)=C1O.I AKMSPOLFRMQWSM-UHFFFAOYSA-N 0.000 description 1
- QZRGKCOWNLSUDK-UHFFFAOYSA-N Iodochlorine Chemical compound ICl QZRGKCOWNLSUDK-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000009938 salting Methods 0.000 description 1
- 150000004961 triphenylmethanes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/06—Hydroxy derivatives of triarylmethanes in which at least one OH group is bound to an aryl nucleus and their ethers or esters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE85929C true DE85929C (https=) |
Family
ID=358020
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT85929D Active DE85929C (https=) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE85929C (https=) |
-
0
- DE DENDAT85929D patent/DE85929C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE85929C (https=) | ||
| DE117767C (https=) | ||
| DE85930C (https=) | ||
| DE268592C (https=) | ||
| DE964238C (de) | Verfahren zur Herstellung von reinen Oxytetracyclinverbindungen | |
| DE406148C (de) | Verfahren zur Darstellung am Stickstoff substituierter Anthranilsaeurederivate | |
| DE574190C (de) | Verfahren zur Herstellung von Kuepenfarbstoffenolschwefelsaeureestern | |
| DE2435222C2 (de) | Verfahren zur Herstellung von N-(2-Diethylamino)-ethyl-2-methoxy-5-methylsulfonylbenzamid | |
| DE236046C (https=) | ||
| DE157554C (https=) | ||
| DE249725C (https=) | ||
| DE188435C (https=) | ||
| DE1543521C (de) | Verfahren zur Herstellung von jodiertem Lecithin | |
| DE58878C (de) | Verfahren zur Darstellung von Dijodthioresorcin | |
| DE92473C (https=) | ||
| DE108128C (https=) | ||
| DE270488C (https=) | ||
| DE217477C (https=) | ||
| DE268451C (https=) | ||
| DE512235C (de) | Verfahren zur Herstellung von Azinderivaten | |
| DE453466C (de) | Verfahren zur Darstellung organischer Arsenverbindungen | |
| DE234851C (https=) | ||
| DE492249C (de) | Verfahren zur Herstellung von Carbonsaeuren am Stickstoff monohalogenierter aromatischer Sulfonamide und von deren Alkali- bzw. Erdalkalisalzen | |
| DE402514C (de) | Verfahren zur Herstellung kolloidalloeslicher Stoffe | |
| DE634285C (de) | Verfahren zur Darstellung von Abkoemmlingen des 2, 4-Dioxotetrahydropyridins |