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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1975617생성일: 2026년 10월 25일

Ciprofloxacin → Ciprofloxacin Hydrochloride Anhydrous

https://huagongshe.com/reaction/1975617

반응식

참여 물질

역할이름HCID투입량
반응물CiprofloxacinHCID 2764—
반응물Sodium ChlorideHCID 5234—
용매WaterHCID 962—
생성물Ciprofloxacin Hydrochloride AnhydrousHCID 62999—

반응 단계

The bandage was placed in a capped vial containing 1 ml of 0.9% NaCl in distilled water at 25° C. After 1 hr of gentle stirring, the aqueous phase was collected and the bandage was placed in a fresh 1 ml portion of 0.9% NaCl. This process was repeated for a total of 24 hour periods. The following procedure for HPLC analysis of ciprofloxacin was essentially that of Darouiche, R. et al, [J. Inf Dis 162, 1124-1125 (1990)]. The conditions were a Whatman Partisil 50D5-3 (C8) column with a mobile phase of 25 ml 0.5M Bu4NHPO4 made up to 2.5 L with distilled water, pH adjusted to 2.34 with 85% H3PO4, which was added to 278 ml HPLC grade acetonitrile, filtered through a 0.2 μ membrane and degassed. The flow rate was 1.5 ml/min at 25° C. with a 500 μl injection loop with detection at 280 nm. Under these conditions ciprofloxacin eluted as a single peak at 9 min. HPLC analysis of the 24 aqueous fractions gave the elution profile shown in Table 2. The data in Table 2 showed that 74% of the initial charge of ciprofloxacin was released in the first 4 hrs. and the release of ciprofloxacin in the subsequent 5 to 24 hrs was remarkably constant. This was thought to be due to the gradual release of ciprofloxacin trapped in the cryogel matrix.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05288503
출처 데이터셋uspto-grants-1994_02
ORD IDord-c3556700e9e94c06b5a4830e83f31804
출처 메모uspto-grants-1994_02