CORCO CHEMICAL CORPORATION

sized structure was then conf irmed by synthesis. Acknowledgment. We would like to ... Write, call or circle the number for more information. CORCO CH...
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Raw Material

i s o l a

Solvent Partition

Ion Exchange HPLC

0.1% Collection Impurity

Reverse Phase HPLC

•KSH

Why there's no better acid than a Corco acid.

•ΕΠΙΖΕβ

•ΕΠΙΖΕβ

iùiZL: Isolated Impurity

Not 6-N-phenyladenine

in

I D E N T I F I C

GC/MS

Synthesis

E

O-pHENYLADENINE

Figure 7. Flow diagram of problem solving

ed adenine derivative and suggest sub­ stitution a t the N-9 position. In an effort to confirm t h e hypothe­ sized structure, 9-phenyladenine was synthesized. Its mass and IR spectra were obtained and compared with spectra of the adenine impurity. T h e infrared spectrum of the synthesized A/-(9-phenyl)adenine is shown in Fig­ ure 6. T h e fingerprint region of this spectrum is identical to that of the isolated impurity. T h e mass spectrum of the synthesized compound was the same as t h a t obtained from the raw material contaminant. Once the impu­ rity was identified, changes were made in t h e production process to ensure t h a t 9-phenyladenine would not be present in the raw material. Identifi­ cation of the impurity and elimination of it as a contaminant in the raw ma­ terial enabled production of adeninefortified blood storage solution to con­ tinue. T h e general scheme and approach to solving this particular problem is shown in the flow diagram in Figure 7. T h e most significant factor is that assumptions were made about the properties of the impurity based on its chromatographic behavior. This in­ formation was then used to make an

educated guess about how best to iso­ late t h e impurity. Furthermore, the data obtained from several different instrumental techniques were com­ bined, and a hypothesized structure of the impurity was fomulated based on the assembled data. T h e hypothe­ sized structure was then confirmed by synthesis. Acknowledgment

We would like to acknowledge L. Streips for analytical work, and A. Berger and S. Scharffenberg for syn­ thetic work.

References

(1) G. B. Bartlett, "Changes of red cell phosphate compounds during storage of human blood in ACD," International Symposium on Erythrocytes, Thrombo­ cytes, Leukocytes, Vienna, 1972, pp 139-148. (2) C. W. Gehrke and D. B. Kaking, J. Chromatogr., 61, 45^63 (1971). (3) J. A. McCloskey, Mass Spectrometry in Nucleic Acid Chemistry, in "Basic Principles in Nucleic Acid Chemistry," P. Tso, Ed., Academic Press, New York, 1974, pp 209-309. (4) Sadtler Research Labs, "Infra-red Spectra, 1969," Spectrum No. 1559.

All Corco acids are certified reagent grade acids. We've been specialists in reagent grade acids since 1953. And we've built our reputation on meeting the requirements and specifications of our customers, ACS and ASTM. Corco can provide reagent grade hydrochloric, nitric, sulfuric acids and sodium hydroxide—plus acetic, fuming nitric, fuming sulfuric, hydrofluoric, perchloric and phosphoric acids. Also bases, solvents and specialty chemicals. When you require the highest purity, you can rely on Corco to deliver. From pints to tank trucks. Write, call or circle the number for more information.

CORCO CORCO CHEMICAL CORPORATION Manufacturers of Reagent & Electronic Chemicals Tyburn Road & Cedar Lane · Fairless Hills, Pa. 19030

(215) 295-5006 CIRCLE 35 ON READER SERVICE CARD

ANALYTICAL CHEMISTRY, VOL. 5 1 , NO. 1 1 , SEPTEMBER

1979 ·

1131 A