Trehalose, dihydrate
6138-23-4O.O.OC[C@H]1O[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1ODPVHGFAJLZWDOC-PVXXTIHASA-NTrehalose dihydrate is an organic molecular entity. It contains a trehalose.
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。
This chemical does not meet GHS hazard criteria for 100% (122 of 122) of all reports.
Not Classified
Aggregated GHS information provided per 122 reports by companies from 2 notifications to the ECHA C&L Inventory.
Chemical: .alpha.-D-Glucopyranoside, .alpha.-D-glucopyranosyl, dihydrate
.alpha.-D-Glucopyranoside, .alpha.-D-glucopyranosyl, dihydrate: Does not have an individual approval but may be used under an appropriate group standard
用途糖研究用。
説明Trehalose is a natural non-reducing disaccharide composed of two α-glucose units. It is found in all major groups of organisms except vertebrates, has biological functions as an osmolyte, storage reserve, and stress protectant, and has diverse commercial applications. Trehalose can also induce or enhance autophagy.
使用D(+)-Trehalose dihydrate is used in many processed foods as well as in biopharmaceutical monoclonal antibody formulations, it is also used as a protein stabilize.
Trehalose is prepared from liquefied starch by a multistep enzymatic process. The commercial product is the dihydrate.
純化方法α,α-D(+)-Trehalose crystallises (as the dihydrate) from aqueous EtOH. Dry it at 13o. For the anhydrous compound dissolve 10g in pyridine (200mL) and distil off this solvent at atmospheric pressure, and when the temperature rises to 115.3o all the H2O is removed and 73mL of distillate is collected. Most of the anhydrous material crystallises out at this stage. The crystals are collected (6.8g), washed with Et2O to give 6.1g of anhydrous product. Higher yields are obtained by slightly more prolonged distillation. [Birch J Chem Soc 3489 1965, X-ray cryst: Brown et al. Acta Cryst 28 3145 1972, Beilstein 17/8 V 3.]
定義本品は、次の化学式で表される二糖類である。
読み込み中…
6138-23-4DTXSID3047972CHEMBL3188936CHEBI:232797