| Document |
Document Title |
|
JPS6045546A |
PURPOSE: To obtain a mixed solution of metallic soap for drier, having high fluidity or excellent storage stability, by mixing a polyoxyalkyl glycol to a solution of a specific metallic organic acid salt mixture and hydrocarbons, and usi...
|
|
JPS5950650B2 |
Cyclopropenoid compounds such as malvalic and sterculic fatty acids found in sterculia oil are rearranged substantially quantitatively to conjugated dienes when heated in the presence of a rhodium catalyst. The dienes can thereafter be r...
|
|
JPS59170165A |
PURPOSE: An ultraviolet curing composition, containing an addition reaction product of a rosin (derivative) with glycidyl acrylate or methacrylate, and suitable for resist ink having improved acid resistance and easy solubility in alkali...
|
|
JPS5935958B2 |
An aqueous process for the recovery of polymeric fatty acids from crystalline clay minerals including catalyst and bleaching clays is provided. The process involves contacting the clay containing the polymeric acid with a sufficient quan...
|
|
JPS5930840B2 |
|
|
JPS59129202A |
PURPOSE: To produce a light-color resin metal salt, by reacting a resin containing carboxyl groups and/or their anhydride groups with a bivalent metal (hydr) oxide or carbonate. CONSTITUTION: 100pts.wt. natural or synthetic resin having ...
|
|
JPS5923358Y2 |
|
|
JPS59104336A |
Aromatic retinoids bearing a trifluoromethoxy substituent on the aromatic nucleus which are useful as antitumor agents and in the treatment of dermatological disorders as well as a method for their manufacture are disclosed.
|
|
JPS5920642B2 |
A new series of substituted esters of 3-hydroxyindone compounds have been found to have exceptional miticidal and herbicidal activity.
|
|
JPS5973435A |
1. Ceric sulphate corresponding to the general overall formula Ce(SO4 )2 . xH2 SO4 . nH2 O (I) in which x and n are greater than or equal to 0 and smaller than or equal to 1 and having a solubility in water, expressed in g/l of cerium in...
|
|
JPS5972445A |
PURPOSE: To obtain a good original image usable as an original printing plate by using the reaction products of rosins and amines as main components, and giving a good binder function and a chargeable function. CONSTITUTION: A compsn. co...
|
|
JPS5915150B2 |
A resinous polyelectrolyte, especially suitable for use as a tackifier in latex adhesives, comprises an ionizable resinous mixture which is ionized with a volatile ionizing agent, said ionizable resinous mixture being the reaction produc...
|
|
JPS5925514U |
|
|
JPS5855129B2 |
2-Substituted or unsubstituted geranyl actic acid esters represented by the general formula [I], [I] wherein R1 represents a hydrogen atom or a hydrocarbon and R5 is the same as R2, R3 or R4 hereinafter defined, are prepared by reacting ...
|
|
JPS58201866A |
PURPOSE: To obtain the titled compound industrially in high yield with the suppressed formation of by-products, e.g. mono- and diglycrides, etc., by reacting rosin with glycidyl ester thereof in the presence of an organic amine under hea...
|
|
JPS58159439A |
Unsaturated acids in rosin or tall oil are disproportionated by heating the rosin or tall oil with a catalyst comprising iodine and an iron compound using ammonia, an ammonium salt or an amine as an additional component of the catalyst. ...
|
|
JPS5835488B2 |
|
|
JPS5835232B2 |
|
|
JPS5833279B2 |
Crude glyceride oils are refined by membrane filtration under pressure in solutions in organic solvents, particularly to separate phosphatides, which may also be refined according to the invention. The solvents are non-acidic, non-hydrox...
|
|
JPS5831297B2 |
|
|
JPS5831298B2 |
|
|
JPS5898371A |
Inert esters of rosin and a primary polyhydric alcohol, such as rosin-pentaerythritol esters, are modified by reacting commercially available rosin esters which contain residual hydroxyl groups with a lower aliphatic carboxylic acid or a...
|
|
JPS5825704B2 |
A method for isomerizing fatty acids which contain an isolated diene structure (-CH=CH-CH2-CH=CH-) and/or disproportionating rosin acids which contain a conjugated diene structure by bringing them in contact with sulfur and/or iodine at ...
|
|
JPS5822491B2 |
There is provided a crystallization-resistant disproportionated rosin prepared by heating a rosin material at temperatures between 250 DEG C. and 275 DEG C. in the presence of from 0.3 percent to 1 percent of specific phenol sulfides, he...
|
|
JPS5822093B2 |
|
|
JPS5821939B2 |
|
|
JPS5821670B2 |
|
|
JPS5817777B2 |
|
|
JPS5817485B2 |
|
|
JPS5812267B2 |
The invention relates to a method for producing metal soaps by reacting aliphatic carboxylic acids with metal oxides, metal hydroxides and/or metal carbonates, wherein the metal soaps are directly obtained in the form of granulates witho...
|
|
JPS588710B2 |
|
|
JPS58478B2 |
|
|
JPS5761077B2 |
|
|
JPS5754067B2 |
|
|
JPS5753827B2 |
|
|
JPS5753392B2 |
|
|
JPS5743112B2 |
1481247 Loss-of-dry inhibitors for oxidizable paints TENNECO CHEMICALS Inc 31 Dec 1974 [21 Jan 1974] 56180/74 Heading C3R A loss-of-dry inhibitor for incorporation in a surface-coating composition containing an oxidizable organic vehicle...
|
|
JPS5742666B2 |
A road marking composition comprising a resin having a melt viscosity of from about 30 to 80 cps at 150 DEG C. and a modifier composed of at least one metal oxide of at least one metal selected from Groups II and IV of short form of the ...
|
|
JPS57141458A |
PURPOSE: To impart a film-forming ability similar to that of enzyme laccase contained in natural Japanese lacquer, by adding to natural Japanese lacquer polyphenol oxidase obtd. from the culture soln. of a strain of the microorganism Alt...
|
|
JPS5736267B1 |
1365695 Mixed calcium salts TENNECO CHEMICALS Inc 26 Oct 1971 [1 Dec 1970] 49670/71 Heading C2C [Also in Division C4] Mixed calcium salts of at least one branchedchain olefinically-unsaturated or saturated aliphatic monocarboxylic acid (...
|
|
JPS5734305B2 |
|
|
JPS5734304B2 |
|
|
JPS57109754A |
The present invention refers to N-Benzoyl- omega -anilinoalkane carboxylic acids, their esters and salts of the general formula
|
|
JPS5728498B2 |
|
|
JPS5720326B2 |
|
|
JPS5652006B2 |
1398926 Treating rosin acids REICHHOLD CHEMICALS Inc 27 June 1972 [23 July 1971] 30081/72 Heading C4D The ethylenic unsaturation of rosin acids is decreased without decarboxylating or otherwise degrading the rosin acids by dispersing int...
|
|
JPS56139572A |
PURPOSE: To obtain seed gum which has high viscosity and excellent transparency and shelf stability and is useful as thickening agents and lusteing agents for various foods, by a method wherein a filter aid is added to a suspension of a ...
|
|
JPS5645518B2 |
|
|
JPS56104836A |
Disclosed is a method of disproportionating rosin comprising heating said rosin in the presence of a dithiin derivative such, for example, as 2,5-diphenyl dithiin. The method can be carried out at about 150 DEG C. to about 300 DEG C. for...
|
|
JPS5665063A |
|
