Acetyltriethyl Citrate
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C14H22O8 318.32
»Acetyltriethyl Citrate contains not less than 99.0percent of C14H22O8,calculated on the anhydrous basis.
Packaging and storage— Preserve in tight containers.
Identification—
B: The retention time for the major peak in the chromatogram of theAssay preparation corresponds to that in the chromatogram of a similar preparation of USP Acetyltriethyl Citrate RS.
Specific gravity á841ñ: between 1.135and 1.139.
Refractive index á831ñ: between 1.432and 1.441.
Acidity— Dissolve 32.0g in 30mLof isopropyl alcohol,previously neutralized to bromothymol blue,add bromothymol blue TS,and titrate with 0.10Nsodium hydroxide to a faint blue endpoint:not more than 1.0mLis required.
Water,Method Iá921ñ: not more than 0.3%.
Assay—
System suitability solution— Prepare a solution in toluene containing about 30mg each of USP Acetyltriethyl Citrate RSand USP Triethyl Citrate RSper mL.
Assay preparation— Transfer about 300mg of Acetyltriethyl Citrate,accurately weighed,to a 10-mLvolumetric flask,dissolve in and dilute with toluene to volume,and mix.
Chromatographic system(see Chromatography á621ñ)— The gas chromatograph is equipped with an on-column,temperature-programmable injector,a flame-ionization detector maintained at about 275,and a 0.32-mm ×30-m column bonded with a 0.5-µm layer of phase G42.The column temperature is programmed to be maintained at about 80for 0.5minute,then to increase to about 220at a rate of 20per minute,and to hold at about 220for 10minutes.The injection port temperature is programmed to be maintained at about 85for 0.5minute,then to increase to about 225at a rate of 20per minute,and to hold at about 225for 10minutes.Helium is used as the carrier gas at a flow rate of about 2.3mLper minute.Chromatograph the System suitability solution,and record the peak responses as directed for Procedure:the relative retention times are about 0.9for triethyl citrate and 1.0for acetyltriethyl citrate;the resolution,R,between triethyl citrate and acetyltriethyl citrate is not less than 1.5;and the relative standard deviation for replicate injections is not more than 2.0%determined from both the triethyl citrate and acetyltriethyl citrate peaks,based on area percent calculation.
Procedure— [NOTE—Use peak areas where peak responses are indicated.]Inject 1µLof theAssay preparation into the chromatograph,record the chromatogram,and measure all of the peak areas,excluding the solvent peak.Calculate the percentage of C14H22O8in the portion of Acetyltriethyl Citrate taken by the formula:
100(A/B),
in whichAis the acetyltriethyl citrate peak response;andBis the sum of the responses of all the peaks.
Auxiliary Information— Staff Liaison:Daniel K.Bempong,Ph.D.,Scientist
Expert Committee:(EMC)Excipients:Monograph Content
USP28–NF23Page 2950
Pharmacopeial Forum:Volume No.27(5)Page 3058
Phone Number:1-301-816-8143