77-59-8C[C@H]1CC[C@]2(NC1)O[C@H]1C[C@H]3[C@@H]4CC[C@H]5C[C@@H](O)CC[C@]5(C)[C@H]4CC[C@]3(C)[C@H]1[C@@H]2CXYNPYHXGMWJBLV-VXPJTDKGSA-NTomatidine is a 3beta-hydroxy steroid resulting from the substitution of the 3beta-hydrogen of tomatidane by a hydroxy group. It is an azaspiro compound, a 3beta-hydroxy steroid and an oxaspiro compound. It is a conjugate base of a tomatidine(1+). It derives from a hydride of a tomatidane.
77-59-8DTXSID0037102CHEMBL2165711CHEBI:9629化学的特性Crystals. Decomposes at 275–280C.
安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
Danger
H301 (50%): Toxic if swallowed [Danger Acute toxicity, oral]
P261, P264, P270, P271, P301+P316, P301+P317, P304+P340, P316, P321, P330, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 2 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
解説(3β,5α,22β,25S)-spirosolan-3-ol.C27H45NO2(415.66).トマチジン,ナス科トマト属Lycopersicumの乾燥葉に,約50% 含まれる配糖体トマチンの加水分解から得られるステロイドアルカロイド.融点202~206 ℃.[α]D+8°(クロロホルム).エタノール,クロロホルム,ピリジンに可溶.トマチン(tomatine,C50H83NO21,融点263~267 ℃,[α]D-19°(ピリジン))は,加水分解によってトマチジンとともにD-グルコース(2分子),D-ガラクトース(1分子),D-キシロース(1分子)を与える.森北出版「化学辞典(第2版)
純化方法Tomatidine forms plates from EtOAc. It is also purified by dissolving 80mg in *C6H6 and applying to an Al2O3 column (3.0g) and eluting with *C6H6, evaporating and recrystallising the residue three times from EtOAc. The hydrochloride has m 265-270o from EtOH and [] D 25 -5o (MeOH). [IR: Uhle J Am Chem Soc 83 1460 1961, Kessar et al. Tetrahedron 27 2869 1971, Schreiber & Adams Experientia 17 13 1961, Beilstein 27 III/IV 1950.]
定義ChEBI: A 3beta-hydroxy steroid resulting from the substitution of the 3beta-hydrogen of tomatidane by a hydroxy group.
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