GB1129546A - Rosin and rosin derivatives processing - Google Patents
Rosin and rosin derivatives processingInfo
- Publication number
- GB1129546A GB1129546A GB44750/66A GB4475066A GB1129546A GB 1129546 A GB1129546 A GB 1129546A GB 44750/66 A GB44750/66 A GB 44750/66A GB 4475066 A GB4475066 A GB 4475066A GB 1129546 A GB1129546 A GB 1129546A
- Authority
- GB
- United Kingdom
- Prior art keywords
- rosin
- rosins
- tall oil
- resorcinol
- thiobis
- 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.)
- Expired
Links
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 title abstract 8
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 title abstract 8
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 title abstract 8
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 8
- 239000003784 tall oil Substances 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 abstract 1
- 101100188555 Arabidopsis thaliana OCT6 gene Proteins 0.000 abstract 1
- 238000005698 Diels-Alder reaction Methods 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- 238000007323 disproportionation reaction Methods 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- -1 hydrogenated rosins Natural products 0.000 abstract 1
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09F—NATURAL RESINS; FRENCH POLISH; DRYING-OILS; OIL DRYING AGENTS, i.e. SICCATIVES; TURPENTINE
- C09F1/00—Obtaining purification, or chemical modification of natural resins, e.g. oleo-resins
- C09F1/02—Purification
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/14—Polysulfides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
- C07C2603/26—Phenanthrenes; Hydrogenated phenanthrenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1,129,546. Treating rosin compounds, tall oil &C. ARIZONA CHEMICAL CO. 6 Oct., 1966 [15 Oct., 1965 (4); 22 June, 1966 (2); 31 Aug., 1966; 16 Sept., 1966 (4)], No. 44750/66. Heading C2C. [Also in Divisions C3 and C4] Rosin compounds, tall oil or tall oil fractions predominating in fatty acids are improved by heating with a compound of the formula where n is at least 1, m is 0 or at least 1, x is 1-3, p is 0 or at least 1, aryl contains 6-18 carbon atoms and R is a hydrocarbon group containing 1-22 carbon atoms. The term " rosin compound " includes tall oil rosins and tall oil fractions predominating in rosin acids, wood and gum rosin, hydrogenated rosins, formaldehyde-treated rosins, Diels-Alder reaction products of rosins, rosin esters, amines, amides and alcohols. The treating agents may be employed in disproportionation reactions. The examples describe the treatment of various rosins, crude and acid-treated and steamdistilled tall oils with agents selected from 2,2- thiobis (4-methyl-6-tert.-butyl phenol), 6-tert.- butyl - o - and - m - cresol) 4,4 - thiobis (resorcinol), 1,1 - thiobis (# - naphthol) and poly- [thio (resorcinol)]. Poly[thio(resorcinol)] is produced by reacting resorcinol in dibutyl ether solution with sulphur dichloride.
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US49665265A | 1965-10-15 | 1965-10-15 | |
| US56084566A | 1966-06-27 | 1966-06-27 | |
| US57621466A | 1966-08-31 | 1966-08-31 | |
| US57981966A | 1966-09-16 | 1966-09-16 | |
| US57985166A | 1966-09-16 | 1966-09-16 | |
| US579817A US3377334A (en) | 1966-09-16 | 1966-09-16 | Disproportionation of rosin |
| US579850A US3377333A (en) | 1965-10-15 | 1966-09-16 | Method of bleaching and stabilization of tall oil during distillation thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1129546A true GB1129546A (en) | 1968-10-09 |
Family
ID=27569814
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB44750/66A Expired GB1129546A (en) | 1965-10-15 | 1966-10-06 | Rosin and rosin derivatives processing |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1129546A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2628762A3 (en) * | 2012-02-20 | 2016-08-24 | Basf Se | Method for manufacturing polyphenol disulfides |
-
1966
- 1966-10-06 GB GB44750/66A patent/GB1129546A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2628762A3 (en) * | 2012-02-20 | 2016-08-24 | Basf Se | Method for manufacturing polyphenol disulfides |
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