| Identification | More | [Name]
Divalproex sodium | [CAS]
76584-70-8 | [Synonyms]
DIVALPROEX SODIUM
Valproate semisodium
SEMISODIUMVALPROATE
Dipropylacetic acid hemisodium salt
Sodium 2-propylpentanoate 2-propylpentanoic acid
SODIUM DIVALPROATE
Valproate Semisodium(Divalproate sodium, Divalproex sodium) | [EINECS(EC#)]
202-303-5 | [Molecular Formula]
C16H31NaO4 | [MDL Number]
MFCD00879852 | [Molecular Weight]
310.4 | [MOL File]
76584-70-8.mol |
| Hazard Information | Back Directory | [Description]
Divalproex is a prodrug form of valproic acid (Item No. 13033) that contains valproic acid and valproate sodium.1 Formulations containing divalproex exhibit delayed gastrointestinal absorption and are converted to valproic acid in the intestine, which reduces gastric irritation and nervous system side effects. Formulations containing divalproex are widely used for the treatment of seizures and bipolar disorder. | [Chemical Properties]
White Solid | [Originator]
Depakote,Abbott | [Uses]
Anticonvulsant; Bipolar Agent | [Uses]
Antiepileptic; Anticonvulsant that also acts as a mood stabilizer for those with bipolar disorder. | [Uses]
Divalproex sodium consists of a compound of sodium valproate and valproic acid in a 1:1 molar relationship in an enteric coated form. In rare cases, it is also used as a treatment for major depressive disorder, and increasingly taken long-term for prevent | [Definition]
ChEBI: A mixture of valproic acid and its sodium salt in a 1:1 molar ratio. It is used for the management and treatment of seizure disorders, mania, and prophylactic treatment of migraine headache. | [Manufacturing Process]
Dipropyl acetic acid or valproic acid may be prepared the next way.
Propylbromide is mixed with cyanacetic acid in the presence of sodium
ethylate, made from absolute ethanol and sodium. By that prepared α,α-
dipropylcyanacetic acid ethyl ester is saponified with equimolecular amounts
of NaOH to give dipropylacetonitril. The desired dipropylacetic acid is produced
by saponification of dipropylacetonitryl with aquatic NaOH. It is colorless
liquid. BP 219°-220°C.
Sodium salt of this acid may be prepared by adding of equivalent of NaOH. | [Brand name]
Depakote (Abbott）. | [Therapeutic Function]
Anticonvulsant | [Clinical Use]
Treatment of manic episodes associated with bipolar disorder
Migraine prophylaxis (unlicensed) | [Drug interactions]
Potentially hazardous interactions with other drugs
Antibacterials: metabolism possibly inhibited
by erythromycin; avoid with pivmecillinam;
concentration reduced by carbapenems - avoid.
Antidepressants: avoid with St John’s wort.
Antiepileptics: concentration reduced by
carbamazepine; concentration of active
carbamazepine metabolite increased; increased
concentration of lamotrigine, phenobarbital,
rufinamide and possibly ethosuximide; sometimes
reduces concentration of active metabolite of
oxcarbazepine; alters phenytoin concentration;
phenytoin and phenobarbital reduce valproate
concentration; hyperammonaemia and CNS toxicity
with topiramate.
Antipsychotics: increased neutropenia with
olanzapine; possibly increases or decreases
concentration of clozapine; possibly increases
quetiapine concentration.
Ciclosporin: variable ciclosporin blood level response.
Sodium oxybate: concentration of sodium oxybate
increased.
Ulcer-healing drugs: metabolism inhibited by
cimetidine, increased concentration. | [Metabolism]
Valproic acid is extensively metabolised in the liver, a large
part by glucuronidation (up to 60
%) and the rest by a
variety of complex pathways (up to 45
%). It is excreted in
the urine almost entirely in the form of its metabolites;
small amounts are excreted in faeces and expired air. |
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