What is the equivalent weight of fumaric acid
Translation of "fumaric acid" in German
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The method of claim 8 wherein the fumaric acid is dissolved in 2-propanol.
The method of claim 8, wherein the Fumaric acid is dissolved in 2-propanol.
The use of fumaric acid for preparing a slow-release pharmaceutical composition.
use of Fumaric acid for the manufacture of a slow-release drug.
Process for producing gamma-butyrolactone by catalytic hydrogenation of maleic acid, fumaric acid and / or succinic acid esters.
Process for the production of gamma -butyrolactone by catalytic hydrogenation of maleic acid, Fumaric acid and / or succinic acid esters.
Copolymers of benzotriazole monomers with maleic or fumaric acid derivatives and polymeric material compositions.
Copolymers of benzotriazole monomers with derivatives of maleic or Fumaric acid and polymeric composition.
An acid addition salt of amlodipine with fumaric acid.
An acid addition salt of amlodipine with Fumaric acid.
The composition of claim 1 wherein the maleic anhydride is converted to fumaric acid.
The composition of claim 1 wherein the maleic anhydride is in Fumaric acid is converted.
Liposomal fumaric acid can be beneficial in the accompanying skin care for the psoriatic skin.
Liposomals Fumaric acid can be helpful in accompanying skin care for psoriasis.
A process as claimed in claim 5, wherein about 1 equivalent of fumaric acid is used.
The method of claim 5 wherein about 1 equivalent Fumaric acid is used.
A preparation according to claim 12 or 13 comprising an amount of the active ingredient corresponding to 10 to 300 mg of fumaric acid.
Preparation according to claim 12 or 13, containing a 10 to 300 mg Fumaric acid corresponding amount of active ingredient.
A method for making the compound of claim 1 comprising contacting bis (POC) PMPA with fumaric acid.
A method of making the compound of claim 1 comprising contacting bis (POC) PMPA with Fumaric acid.
The binder resin according to claim 2, wherein said compound reacting with both monomers is selected from fumaric acid, acrylic acid, and methacrylic acid.
The binder resin of claim 2, wherein the compound reactive with both monomers is selected from Fumaric acid, Acrylic acid and methacrylic acid is selected.
The method of Claim 19 wherein malic or fumaric acid is added to the fermentation broth before its introduction into the fluidized bed reactor.
The method of claim 19, wherein apples or Fumaric acid is added to the fermentation broth prior to introducing it into the fluidized bed reactor.
A pharmaceutical composition as claimed in claim 10 for delivering the residue of fumaric acid and / or one or more amino acids to humans.
Medicinal preparation according to claim 10 for dispensing the residues of Fumaric acid and / or one or more amino acid (s) in humans.
A process according to Claim 5 wherein a radical former is used for grafting the fumaric acid to the polyolefin.
Process according to Claim 5, characterized in that the Fumaric acid a radical generator is used on the polyolefin.
A process of Claim 1, wherein the acidulent antimicrobial agent is selected from fumaric acid and citric acid.
The method of claim 1 in which the antimicrobial acidulant is selected from Fumaric acid and citric acid.
The bathing preparation as claimed in claim 1, wherein said fumaric acid is that treated with at least 0.2% by weight of polyethylene glycol.
Bath preparation according to claim 1, wherein the Fumaric acid is treated with at least 0.2 wt.% polyethylene glycol.
Process for production of l-aspartic acid from fumaric acid with aspartase
Process for the production of aspartic acid from Fumaric acid with aspartase
Topical cosmetic and pharmaceutical composition comprising specific alkoxylated diester of fumaric acid
Topical cosmetic and pharmaceutical compositions containing specific alkoxylated diesters of Fumaric acid
A composition according to claim 5 where said inhibitor is selected from the group consisting of acetylenic hydrocarbons and alcohols, tertiary amines and esters of maleic and fumaric acid.
The composition of claim 5, wherein the inhibitor compound is selected from acetylenic hydrocarbons and alcohols, tertiary amines and esters of maleic acid and Fumaric acid is selected.
A process as claimed in any of claims 1 to 3, wherein the secondary components (2) contain acetic acid, maleic acid, fumaric acid and / or formaldehyde.
Process according to one of Claims 1 to 3, characterized in that the secondary components (2) acetic acid, maleic acid, Fumaric acid and / or formaldehyde.
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