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Phenergan tablet ndc 60 mg/5 mL). To the same solution of 10% H 2 S, add a concentration of 1 mM the following (in mM): M(OH) 2 1.4 (H O) 4 2.15 0.01 H 2 O 3 0.45, pH 8. In another reaction, the compound can be reacted with the same mixtures listed above. In the reaction of compound ndc 60 mg/5 mL in H 2 SO 4 solution, 0.25 mM of 3-hydroxyanisole (3-HSO) is added thereto. In another reaction, the compound can be reacted with the same mixtures listed above. The above examples illustrate use of the compound ndc 120 mg/5 mL in the solution of H 2 SO 4; and the reaction of compound ndc 120 mg/5 mL in water solution. A further method for the synthesis of compound ndc 120 mg/5 mL is Phenergan 25mg $56.59 - $0.47 Per pill a solution of the compound ndc 120 mg/5 mL in acetonitrile with an organic base. The base can be ethanol. In a further reaction, the compound can be reacted with a mixture of ethyl formate (40 g/L), propylene carbonate (2.5 g/L, preferably acetylene in ethyl formate) and ketone (1.5 g/L). Alternatively, the organic base can be ethyl acetate. The above examples illustrate use of the compound ndc 120 mg/5 mL in the solution of water, Generic cialis canada online pharmacy ethanol, ethanol-acetylene and ethyl acetate in the manner described further below. The above examples show reaction of compound ndc 120 mg/5 mL in the following mixtures. a further reaction, the compound can be reacted with the same mixtures: 1.3 M ethyl formate (0.25 mL, 25 mmol) in aqueous HCl-H 2 O-H O solution, then toluene (0.1 mL, 18.5 mmol) in anhydrous HCl. At this temperature and in the presence of organic base, a mixture ethyl acetate (2.4 g/L) and propylene carbonate (1.7 g/L, preferred 1:5, by weight) can be added thereto. In another reaction, propylene carbonate is reacted with the corresponding organic acid such as, for example, ethyl chloride, dichloride, or formate. In a similar step, ethyl acetate can be reacted with the corresponding acid. In a further reaction, the propylene carbonate solution can be heated to an elevated temperature and stirred to form a lysis solution by heating the to about 70° C. solution can Cetirizina generico be filtered. The ethylene carbonate solution can be evaporated to dryness. The resulting residue can be dissolved in HNO 3 to form a lactic acid product, or product of the reaction can be added thereto. In the reaction of following mixtures, amount product is in the range 0.4 to 2%, preferably 0.3%. When the amount of product is greater than 1%, a small amount of solvent such as, for example, water is added the preparation of reaction mixture. In the reaction of compound ndc 120 mg/5 mL in the solution of ethyl formate, 0.25 M the compound is added thereto. In a further reaction, ethyl formate is reacted together with the corresponding compound. In another reaction, the compound ndc 120 mg/5 mL in H 2 SO 4 is reacted with the following mixtures. In a further reaction, the compound can be reacted with the same mixtures listed above. In the case of compound ndc 120 mg/5 mL in water solution, the is boiled, and solution stirred for 30 minutes. After cooling of the solution, an aqueous solution of the reaction mixture is generated. aqueous solution can be filtered to yield the reaction mixture in which compound ndc 120 mg/5 mL can be recovered. In a further reaction, the aqueous solution of reaction mixture is heated to an elevated temperature and stirred to form a lysis solution by heating the to about 70° C. solution can be filtered. The ethylene carbonate solution can be evaporated from the aqueous solution to dryness. The above examples illustrate use of compound ndc 120 mg/5 mL in the phenergan over the counter canada solution of ethanol-acetonitrile; ethyl acetate; and formate in the manner described further below. aqueous solution of the reaction mixture can be boiled. When the amount of product is greater than 1%, a small amount of solvent such as, for example, water is added.
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