GB919720A - Hemi-acetals, their preparation and use - Google Patents
Hemi-acetals, their preparation and useInfo
- Publication number
- GB919720A GB919720A GB25593/60A GB2559360A GB919720A GB 919720 A GB919720 A GB 919720A GB 25593/60 A GB25593/60 A GB 25593/60A GB 2559360 A GB2559360 A GB 2559360A GB 919720 A GB919720 A GB 919720A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxy
- group
- aldehyde
- hydrogen
- groups
- 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
- 150000002373 hemiacetals Chemical class 0.000 title abstract 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 8
- 150000001299 aldehydes Chemical class 0.000 abstract 5
- -1 alkylene radical Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 abstract 3
- GXANMBISFKBPEX-ONEGZZNKSA-N (e)-hex-3-enal Chemical compound CC\C=C\CC=O GXANMBISFKBPEX-ONEGZZNKSA-N 0.000 abstract 2
- HSJKGGMUJITCBW-UHFFFAOYSA-N 3-hydroxybutanal Chemical compound CC(O)CC=O HSJKGGMUJITCBW-UHFFFAOYSA-N 0.000 abstract 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 abstract 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 abstract 2
- 125000003172 aldehyde group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- MMFCJPPRCYDLLZ-UHFFFAOYSA-N dec-2-enal Chemical compound CCCCCCCC=CC=O MMFCJPPRCYDLLZ-UHFFFAOYSA-N 0.000 abstract 2
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 abstract 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 abstract 2
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- BSABBBMNWQWLLU-UHFFFAOYSA-N lactaldehyde Chemical compound CC(O)C=O BSABBBMNWQWLLU-UHFFFAOYSA-N 0.000 abstract 2
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 150000003254 radicals Chemical class 0.000 abstract 2
- DTCCTIQRPGSLPT-ONEGZZNKSA-N (E)-2-pentenal Chemical compound CC\C=C\C=O DTCCTIQRPGSLPT-ONEGZZNKSA-N 0.000 abstract 1
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 abstract 1
- OMLOASXVBUNPTN-UHFFFAOYSA-N 2,4-dimethylcyclohexane-1-carbaldehyde Chemical compound CC1CCC(C=O)C(C)C1 OMLOASXVBUNPTN-UHFFFAOYSA-N 0.000 abstract 1
- LELITMWJHWIJIF-UHFFFAOYSA-N 2-hydroxy-3-sulfanyltetradecanal Chemical compound OC(C=O)C(CCCCCCCCCCC)S LELITMWJHWIJIF-UHFFFAOYSA-N 0.000 abstract 1
- UIKQNMXWCYQNCS-UHFFFAOYSA-N 2-hydroxybutanal Chemical compound CCC(O)C=O UIKQNMXWCYQNCS-UHFFFAOYSA-N 0.000 abstract 1
- VTERBIYJBWDXDT-UHFFFAOYSA-N 2-hydroxybutanedial Chemical compound O=CC(O)CC=O VTERBIYJBWDXDT-UHFFFAOYSA-N 0.000 abstract 1
- WWMIMRADNBGDHP-UHFFFAOYSA-N 2-hydroxyhexanedial Chemical compound O=CC(O)CCCC=O WWMIMRADNBGDHP-UHFFFAOYSA-N 0.000 abstract 1
- JEGJNDOQGGWGNL-UHFFFAOYSA-N 2-sulfanylhexanal Chemical compound CCCCC(S)C=O JEGJNDOQGGWGNL-UHFFFAOYSA-N 0.000 abstract 1
- AKXKFZDCRYJKTF-UHFFFAOYSA-N 3-Hydroxypropionaldehyde Chemical compound OCCC=O AKXKFZDCRYJKTF-UHFFFAOYSA-N 0.000 abstract 1
- IPKHBLZYXAFQNZ-UHFFFAOYSA-N 3-aminodecanal Chemical compound CCCCCCCC(N)CC=O IPKHBLZYXAFQNZ-UHFFFAOYSA-N 0.000 abstract 1
- ORWWURAJRKRYBY-UHFFFAOYSA-N 3-aminopentanal Chemical compound CCC(N)CC=O ORWWURAJRKRYBY-UHFFFAOYSA-N 0.000 abstract 1
- PCXDJQZLDDHMGX-UHFFFAOYSA-N 3-aminopropanal Chemical compound NCCC=O PCXDJQZLDDHMGX-UHFFFAOYSA-N 0.000 abstract 1
- RQVFCBDGGZQMDN-UHFFFAOYSA-N 3-ethyl-5-methylheptanal Chemical compound CCC(C)CC(CC)CC=O RQVFCBDGGZQMDN-UHFFFAOYSA-N 0.000 abstract 1
- XZCHSPPQZUOKRM-UHFFFAOYSA-N 3-hydroxycyclohexane-1-carbaldehyde Chemical compound OC1CCCC(C=O)C1 XZCHSPPQZUOKRM-UHFFFAOYSA-N 0.000 abstract 1
- USJRMLZTONLKON-UHFFFAOYSA-N 3-sulfanylbutanal Chemical compound CC(S)CC=O USJRMLZTONLKON-UHFFFAOYSA-N 0.000 abstract 1
- DLKSIGNUTFOJIC-UHFFFAOYSA-N 3-sulfanylpentanal Chemical compound CCC(S)CC=O DLKSIGNUTFOJIC-UHFFFAOYSA-N 0.000 abstract 1
- BMYLOHDOJPEVOR-UHFFFAOYSA-N 3-sulfanylpropanal Chemical compound SCCC=O BMYLOHDOJPEVOR-UHFFFAOYSA-N 0.000 abstract 1
- UMHJEEQLYBKSAN-UHFFFAOYSA-N Adipaldehyde Chemical compound O=CCCCCC=O UMHJEEQLYBKSAN-UHFFFAOYSA-N 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 abstract 1
- 229930040373 Paraformaldehyde Natural products 0.000 abstract 1
- PCSMJKASWLYICJ-UHFFFAOYSA-N Succinic aldehyde Chemical compound O=CCCC=O PCSMJKASWLYICJ-UHFFFAOYSA-N 0.000 abstract 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 abstract 1
- 230000002378 acidificating effect Effects 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- DTCCTIQRPGSLPT-UHFFFAOYSA-N beta-Aethyl-acrolein Natural products CCC=CC=O DTCCTIQRPGSLPT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 abstract 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 abstract 1
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 abstract 1
- XPCJYQUUKUVAMI-UHFFFAOYSA-N cyclohex-2-ene-1-carbaldehyde Chemical compound O=CC1CCCC=C1 XPCJYQUUKUVAMI-UHFFFAOYSA-N 0.000 abstract 1
- KVFDZFBHBWTVID-UHFFFAOYSA-N cyclohexanecarbaldehyde Chemical compound O=CC1CCCCC1 KVFDZFBHBWTVID-UHFFFAOYSA-N 0.000 abstract 1
- 239000003822 epoxy resin Substances 0.000 abstract 1
- 229940015043 glyoxal Drugs 0.000 abstract 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- OADYBSJSJUFUBR-UHFFFAOYSA-N octanedial Chemical compound O=CCCCCCCC=O OADYBSJSJUFUBR-UHFFFAOYSA-N 0.000 abstract 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 abstract 1
- 229920002866 paraformaldehyde Polymers 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 229920000647 polyepoxide Polymers 0.000 abstract 1
- 229920001228 polyisocyanate Polymers 0.000 abstract 1
- 239000005056 polyisocyanate Substances 0.000 abstract 1
- 239000002243 precursor Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 239000012260 resinous material Substances 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
- 125000003396 thiol group Chemical group [H]S* 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/47—Condensation polymers of aldehydes or ketones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D323/00—Heterocyclic compounds containing more than two oxygen atoms as the only ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B31/00—Preparation of derivatives of starch
- C08B31/003—Crosslinking of starch
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3206—Polyhydroxy compounds aliphatic
- C08G18/3209—Aliphatic aldehyde condensates and hydrogenation products thereof
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/56—Polyacetals
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/24—Di-epoxy compounds carbocyclic
- C08G59/245—Di-epoxy compounds carbocyclic aromatic
-
- C—CHEMISTRY; METALLURGY
- C14—SKINS; HIDES; PELTS; LEATHER
- C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
- C14C3/00—Tanning; Compositions for tanning
- C14C3/02—Chemical tanning
- C14C3/08—Chemical tanning by organic agents
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/12—Aldehydes; Ketones
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/137—Acetals, e.g. formals, or ketals
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/06—Alcohols; Phenols; Ethers; Aldehydes; Ketones; Acetals; Ketals
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/09—Polyolefin
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/10—Polyvinyl halide esters or alcohol fiber modification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Textile Engineering (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paper (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US829211A US3183054A (en) | 1959-07-24 | 1959-07-24 | Aldehyde condensation products and their use in treating fibrous materials |
| US3988A US3080281A (en) | 1959-07-24 | 1960-01-22 | Hydroxy-containing hemi-acetals, their preparation and use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB919720A true GB919720A (en) | 1963-02-27 |
Family
ID=26672451
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB25593/60A Expired GB919720A (en) | 1959-07-24 | 1960-07-22 | Hemi-acetals, their preparation and use |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US3183054A (enExample) |
| BE (1) | BE593301A (enExample) |
| CH (1) | CH433226A (enExample) |
| ES (1) | ES259814A1 (enExample) |
| GB (1) | GB919720A (enExample) |
| MY (1) | MY6400130A (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE593301A (enExample) * | 1959-07-24 | |||
| BE617614A (enExample) * | 1961-05-18 | |||
| US3189403A (en) * | 1963-06-19 | 1965-06-15 | Windus Wallace | Tanning with a hemiacetal and resorcinol or pyrogallol solution |
| DE1233817B (de) * | 1963-10-03 | 1967-02-09 | Pfersee Chem Fab | Verfahren zur Hochveredlung von Textilmaterialien, die natuerliche und/oder regenerierte Cellulosefasern enthalten |
| US3441367A (en) * | 1965-12-22 | 1969-04-29 | Us Agriculture | Method for setting finishes on cellulosic textiles with catalyst composition of magnesium halide and organic acid |
| US3443987A (en) * | 1965-12-29 | 1969-05-13 | Shell Oil Co | Process for treating fibrous material with aldehyde condensation products and the resulting material |
| US3535141A (en) * | 1967-04-17 | 1970-10-20 | Deering Milliken Res Corp | Process for making sail release synthetic textile |
| US3645667A (en) * | 1970-05-22 | 1972-02-29 | Us Agriculture | Nonaqueous cross linking of cellulose with a methylolated urea in the absence of an acidic catalyst |
| US4210755A (en) * | 1970-12-24 | 1980-07-01 | L'oreal | Aminated γ-dialdehyde; methods for preparing the same and cosmetic compositions containing the same |
| US4014990A (en) * | 1970-12-24 | 1977-03-29 | Societe Anonyme Dite: L'oreal | Animated-γ-dialdehydes in hair strengthening compositions |
| AR196921A1 (es) * | 1972-04-01 | 1974-02-28 | Basf Ag | Procedimiento para la obtencion de formulaciones curtientes |
| US3867198A (en) * | 1973-06-13 | 1975-02-18 | Formica Corp | Method of cleaning the surface of a decorative plastic laminate |
| US4167500A (en) * | 1976-06-14 | 1979-09-11 | Lord Corporation | Aqueous compositions comprising phenolic resin and crosslinking agent |
| US4447241A (en) * | 1982-04-12 | 1984-05-08 | Springs Industries, Inc. | Oxidative afterwash treatment for crease resisting fabrics |
| US4508594A (en) * | 1984-06-28 | 1985-04-02 | Nalco Chemical Company | Polyaldehyde/polyacetal compositions |
| DE3811267C1 (enExample) * | 1988-04-02 | 1989-05-18 | Schill & Seilacher Gmbh & Co, 7030 Boeblingen, De | |
| ATE126556T1 (de) | 1990-02-01 | 1995-09-15 | James River Corp | Durch die vernetzung von holzstoffasern mit polykarbonsäuren erhaltene elastische, voluminöse faser. |
| DE4102545A1 (de) * | 1991-01-29 | 1992-07-30 | Basf Ag | Verfahren zum alleingerben, vorgerben und mitgerben von bloessen und fellbloessen und zum nachgerben von leder und fell |
| TW223103B (enExample) * | 1992-02-03 | 1994-05-01 | Ciba Geigy Ag | |
| US6165321A (en) * | 1998-04-28 | 2000-12-26 | Penford Corporation | Method of sizing substrates |
| AU2003232247A1 (en) * | 2002-05-07 | 2003-11-11 | Basf Aktiengesellschaft | Tanning agent and curing agent based on dialdehydes |
| DE102017123020A1 (de) * | 2017-10-04 | 2019-04-04 | Tfl Ledertechnik Gmbh | Zusammensetzung und Verfahren zur Gerbung |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2078534A (en) * | 1935-05-25 | 1937-04-27 | Shell Dev | Cyclic acetals and process for producing same |
| BE438129A (enExample) * | 1939-03-04 | |||
| US2696477A (en) * | 1951-04-21 | 1954-12-07 | Dan River Mills Inc | Acrolein-formaldehyde condensation product |
| US2771337A (en) * | 1952-05-03 | 1956-11-20 | Dan River Mills Inc | Acrolein-formaldehyde condensation products and process of applying the same to cellulose fabric |
| BE534687A (enExample) * | 1954-01-08 | |||
| BE593301A (enExample) * | 1959-07-24 |
-
0
- BE BE593301D patent/BE593301A/xx unknown
-
1959
- 1959-07-24 US US829211A patent/US3183054A/en not_active Expired - Lifetime
-
1960
- 1960-01-22 US US3988A patent/US3080281A/en not_active Expired - Lifetime
- 1960-07-22 CH CH465261A patent/CH433226A/de unknown
- 1960-07-22 ES ES0259814A patent/ES259814A1/es not_active Expired
- 1960-07-22 GB GB25593/60A patent/GB919720A/en not_active Expired
-
1964
- 1964-12-31 MY MY1964130A patent/MY6400130A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CH433226A (de) | 1967-04-15 |
| US3080281A (en) | 1963-03-05 |
| ES259814A1 (es) | 1960-12-16 |
| MY6400130A (en) | 1964-12-31 |
| US3183054A (en) | 1965-05-11 |
| BE593301A (enExample) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4126640A (en) | N-alkyl polyamines and curing of epoxy resins therewith | |
| US2938884A (en) | Oxypropylation of phenolic resins | |
| US2842523A (en) | Beta-amino lower-alkyl carbamates and resinous reaction products thereof | |
| US4195152A (en) | N-Alkyl polyamines and curing of epoxy resins therewith | |
| US2545692A (en) | Resin-forming reaction of phenol, aldehyde, and amine in presence of polyhalophenol | |
| US2966478A (en) | Diimidazoline from c19 dibasic acid | |
| US3361821A (en) | Mixture of nonadecane diamines | |
| US3303165A (en) | Diamine curing agent for epoxy resins | |
| US4990576A (en) | Tetramines by amination of polyoxyalkylene glycols | |
| US5120817A (en) | Epoxy resin compositions | |
| US3546172A (en) | Ethylene urea terminated phenolic resins | |
| US3063959A (en) | Aldol condensation product-phenol aldehyde condensation product and method for making same | |
| US2485711A (en) | Phenol aldehyde resins | |
| US2486392A (en) | Alkylfuran resins and method of making same | |
| US3494889A (en) | Bisphenol-epichlorohydrin resins cured with alkylidenebis (alpha,alpha' - diamino - 2,6-xylenols) | |
| GB597144A (en) | Improvements in or relating to synthetic resinous adhesive compositions | |
| GB603872A (en) | Improvements in and relating to polyformals | |
| GB1045187A (en) | Bisphenolic lactones | |
| US2631991A (en) | Pyrazoline resins | |
| US5068444A (en) | Tetramines by amination of dialdehyde glycol adducts | |
| US3322740A (en) | Alkylene oxide-polyol polyether modified acetal resins | |
| GB958517A (en) | Novel polyepoxyaldehydes and process for making them | |
| US2907733A (en) | Diphenolic acid modified oil-aldehyde condensates | |
| JPS6368623A (ja) | フエノ−ル樹脂組成物の製造法 | |
| US2710852A (en) | Resins from cyanoacyl hydrazides |