Detail of > 3521-62-8
- CAS Number:
- 3521-62-8
- Name:
Erythromycin estolate
- Formula:
- C52H97NO18S
- Molecular Structure:

- Synonyms:
- Sulfuricacid, monododecyl ester;LP 35;Lauryl alcohol sulfate;Lauryl hydrogen sulfate;
- Molecular Weight:
- 1056.39
- EINECS:
- 222-532-4
- Melting Point:
- 135-140 °C dec.
- Boiling Point:
- 827.7 °C at 760 mmHg
- Flash Point:
- 454.4 °C
- Appearance:
- Long needles
- Hazard Symbols:
Xn,
Xi- Risk Codes:
- 22-42/43-36/37/38
- Safety:
- 22-36-26Details
- Deleted CAS:
- 12167-63-4|28375-06-6|31261-46-8
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Reference
- Effect of food intake on the action of orally administered drugs
- Effect of food intake on the action of orally administered drugs. 6. Takano, Masahiko (Tokyo Henshin Hosp., Tokyo, Japan). Gekkan Yakuji, 18(11), 2003-9 (Japanese) 1976. CODEN: YAKUD5. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) The efficacy of erythromycin (I) [114-07-8] in patients was greater when I was given before rather than after meals, whereas that of erythromycin estolate [3521-62-8] or triacetyloleandomycin [2751-09-9] was not influenced by food intake.There are some commonly used reagents with their cas registry numbers 643-22-1 and 114-07-8 in this article. Some data supported that erythromycin stearate [643-22-1] should be administered before meals but others indicated that it could be given after meals. .
- A simple thin-layer chromatographic identification procedure for erythromycin base, stearate, estolate and ethylsuccinate
- A simple thin-layer chromatographic identification procedure for erythromycin base, stearate, estolate and ethylsuccinate. Vilim, A.; LeBelle, M. J.; Wilson, W. L.; Graham, K. C. (Drug Res. Lab., Health Welfare Canada, Ottawa, Ont., Can.). J. Chromatogr. 1264-62-6 and 57-68-1 are cas registry numbers of chemicals which are used as reagents here., 133(1), 239-44 (English) 1977. CODEN: JOCRAM. DOCUMENT TYPE: Journal CA Section: 64 (Pharmaceutical Analysis) Erythromycin (I) [114-07-8], I estolate [3521-62-8], I Et succinate [1264-62-6], and I stearate [643-22-1] were differentiated by thin-layer chromatog. using silica gel 60 F254-coated plates, MeOH, 90%10%1 CHCl3-MeOH-HOAc, and 90%5%5 MeOH-CHCl3-HOAc solvent systems, and a K2Cr2O7-H2SO4 detection reagent. The method was used to detect the compds. in 8 formulations, with no excipient interference occurring. The system can also detect sulfadiazine [68-35-9], sulfamerazine [127-79-7], and sulfamethazine [57-68-1] in a I estolate formulation. .
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