Detail of > 862-89-5
- CAS Number:
- 862-89-5
- Name:
Estr-4-en-3-one,17-[(1-oxoundecyl)oxy]-, (17b)-
- Superlist Name:
- Nandrolone undecylate
- Formula:
- C29H46O3
- Molecular Structure:
![Molecular Structure of 862-89-5 (Estr-4-en-3-one,17-[(1-oxoundecyl)oxy]-, (17b)-)](http://www.lookchem.com/300w/2010/0624/862-89-5.jpg)
- Synonyms:
- Estr-4-en-3-one,17b-hydroxy-, undecanoate (7CI,8CI);Undecanoic acid, ester with 17b-hydroxyestr-4-en-3-one (8CI);Dynabolon;Nandrolone-17b-undecanoate;
- Molecular Weight:
- 442.68
- EINECS:
- 212-729-3
- Density:
- 1.04 g/cm3
- Boiling Point:
- 548.5 °C at 760 mmHg
- Flash Point:
- 230.6 °C
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Reference
- Nandrolone 17
- Nandrolone 17.beta.-ester-containing drugs with anabolic activity. Van der Vies, Johannes (AKZO N. V., Neth.). Ger. Offen. DE 2638507 3 Mar 1977, 16 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: A61K031-565. PRIORITY: NL 75-10104 27 Aug 1975. DOCUMENT TYPE: Patent CA Section: 63 (Pharmaceuticals) Oral compns.Several reagents with their cas registry numbers 1491-81-2 and 62541-10-0 are used here. with anabolic activity comprise .ltoreq.50% of a 17.beta.-ester (I) of nandrolone and a C9-18 aliph. carboxylic acid in a nonsteroidal lipid carrier. For example, 5g nandrolone was dissolved in 50 mL pentane and 5mL pyridine and esterified with 5 mL .alpha.-methylcapric acid to give 6.3 g nandrolone 17.beta.-.alpha.-methylcaprate [62516-28-3]. Soft gelatin capsules (0.12 mL) were filled with a sterile soln. of 83.33 g/L nandrolone 17.beta.-undecanoate (II) [862-89-5] in peanut oil so that each capsule contained 10 mg II. Tablets and hard gelation capsules contg. the nandrolone esters and lipid carriers were also prepd. .
- Analysis of nandrolone esters in oily injections by reversed-phase high-performance liquid chromatography
- Analysis of nandrolone esters in oily injections by reversed-phase high-performance liquid chromatography.Some chemicals with cas registry numbers like 862-89-5 and 100-52-7 are also used. Cavrini, V.; Di Pietra, A. M.; Raggi, M. A.; Sarti, R. (Ist. Chim. Farm. Tossicol., Bologna 40126, Italy). J. Pharm. Biomed. Anal., 5(1), 21-32 (English) 1987. CODEN: JPBADA. ISSN: 0731-7085. DOCUMENT TYPE: Journal CA Section: 64 (Pharmaceutical Analysis) A HPLC procedure is presented for the anal. of nandrolone esters [I, R = (CH2)2Ph; (CH2)8Me and (CH2)9Me] in com. oily injections. The anal. was carried out under isocratic, reversed-phase (RP8 column) conditions using a UV detector (240 nm). The system discriminates between nandrolone alc., a potential impurity, and its esters and permits the quantitation of trace benzaldehyde [100-52-7] derived from the oxidative degrdn. of benzyl alc. [100-51-6]. The proposed HPLC method was more specific and accurate than the pharmacopeial spectrophotometric assay procedure (isoniazid reagent). The interference of benzaldehyde with the isoniazid method was also investigated. .
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