Detail of > 57-87-4
- CAS Number:
- 57-87-4
- Name:
Ergosta-5,7,22-trien-3-ol,(3b,22E)-
- Superlist Name:
- Ergosterol
- Formula:
- C28H44O
- Molecular Structure:

- Synonyms:
- Ergosterol (8CI);(22E,24R)-Ergosta-5,7,22-trien-3b-ol;(24R)-Ergosta-5,7,22-trien-3b-ol;24-Methylcholesta-5,7,22-trien-3b-ol;24R-Methylcholesta-5,7,22E-trien-3b-ol;24a-Methyl-22E-dehydrocholesterol;3b-Hydroxyergosta-5,7,22-triene;Ergosterin;Provitamin D2;Reishi Mushroom PE;
- Molecular Weight:
- 396.65
- EINECS:
- 200-352-7
- Density:
- 1 g/cm3
- Melting Point:
- 156-158 °C(lit.)
- Boiling Point:
- 501.5 °C at 760 mmHg
- Flash Point:
- 216.3 °C
- Hazard Symbols:
T+- Risk Codes:
- 28-48/20/22-40-38
- Safety:
- 28-36/37-45Details
- Transport Information:
- UN 2811 6.1/PG 2
- Deleted CAS:
- 18844-74-1|37571-51-0
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Reference
- Resistance to fungicides which inhibit ergosterol biosynthesis in laboratory strains of Botrytis cinerea and Ustilago maydis
- Resistance to fungicides which inhibit ergosterol biosynthesis in laboratory strains of Botrytis cinerea and Ustilago maydis. Leroux, Pierre; Gredt, Michel (Stn. Phytopharm., INRA, Versailles 78000, Fr.). Pestic. Sci., 15(1), 85-9 (English) 1984. CODEN: PSSCBG. ISSN: 0031-613X. 60029-23-4 and 63284-71-9 which are cas registry numbers are also used here. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemical Bioregulators) Section cross-reference(s): 10 The strains of B. cinerea or U. maydis selected on fenarimol [60168-88-9], triarimol [26766-27-8] or triadimefon [43121-43-3] were also resistant to the other inhibitors of sterol C-14 demethylation; the sterol compn. of the strains was normal. Among the isolates of U. maydis resistant to dodemorph [1593-77-7], fenpropidine [67306-00-7], fenpropemorph [67306-03-0], and tridemorph [81412-43-3], some were resistant to the 15-azasteroid A 25822B [50686-98-1] and did not contain ergosterol [57-87-4]. The other strains remained sensitive to A 25822B and had a normal sterol compn. All the resistant isolates and the wild-type were inhibited to the same extent by nystatin [1400-61-9] and pimaricin [7681-93-8]. .
- Influence of choline derivatives on the sterol composition of Chlorella vulgaris grown in continuous culture
- Influence of choline derivatives on the sterol composition of Chlorella vulgaris grown in continuous culture. Orcutt, D. M.; Davis, G. A.; Moore, L. D. (Dep. Plant Pathol. Physiol., Virginia Polytech. Inst. and State Univ., Blacksburg, VA 24061, USA). Can. J. Bot., 62(1), 78-80 (English) 1984. CODEN: CJBOAW. ISSN: 0008-4026. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemical Bioregulators) CCC [999-81-5], (2-hydroxyethyl)trimethylammonium chloride (CC) [67-48-1], and (2-hydroxyethyl)trimethylammonium chloride phosphate (PCC) [107-73-3] decreased ergosterol (I) [57-87-4], as a percentage of total sterol extd. from C. vulgaris cells grown in continuous culture. Each compd. was tested sequentially at 10-6, 10-5, and 10-4 M. The greatest redn. in the relative percentage of I occurred with 10-4M CC. CCC and PCC treatment increased the relative percentage of 22-dihydroergosterol [516-79-0], yet no accumulation of 22-dihydroergosterol was obsd. with the CC treatments. All 3 chems. increased the relative amts. of C27 sterols. Abs. concns. of total sterols were significantly reduced by CC at 10-6 and 10-4 M. 434-16-2 and 516-79-0 are just another two chemicals used in this study. CC, at 10-5 M, significantly increased abs. concns. of total sterols as did PCC at 10-6 and 10-5 M. .
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