Salicyl Alcohol
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90-01-7OCc1ccccc1OCQRYARSYNCAZFO-UHFFFAOYSA-NSalicyl alcohol is a hydroxybenzyl alcohol that is phenol substituted by a hydroxymethyl group at C-2. It has a role as a human urinary metabolite. It is a hydroxybenzyl alcohol and an aromatic primary alcohol. It is functionally related to a phenol and a benzyl alcohol.
90-01-7DTXSID9045843CHEMBL280802CHEBI:16464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 35.2% (37 of 105) of reports.
Warning
H315 (64.8%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 105 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Chemical: Benzenemethanol, 2-hydroxy-
Benzenemethanol, 2-hydroxy-: Does not have an individual approval but may be used under an appropriate group standard
Used in phenol-formaldehyde resols; [Kanerva, p. 1815]
Plastic Composites Manufacturing [Category: Industry]
解説サリチルアルコール.サリゲニン(saligenin)ともいう.フェノール配糖体サリシンのアグリコンで,これを加水分解すると得られる.また,サリチルアルデヒドの還元により合成できる.白色の結晶.融点86~87 ℃.100 ℃ で昇華する.水,エタノール,エーテルなどに可溶.塩化鉄(Ⅲ)により青色を呈する.
使用2-Hydroxybenzyl Alcohol is a phenolic component of a part of a salix bark extract which maintains a minor anti-depressant effect. Phenolic analog with potential for anti-melanomic effect. Also It is an intermediate in the production of phenol formaldehyde res ins (may remain after condensation of the resin); sensitizer in phenol-formaldehyde resins; in loeal anesthetics.
一般的な説明2-Hydroxybenzyl alcohol participates in the selective ring opening reaction of 4H-1,3,2-benzodioxasilines.
純化方法Crystallise saligenine from water or EtOH/*C6H6 (m 89o). [Beilstein 6 III 4537, 6 IV 5896.]
読み込み中…
化学的特性light brown crystalline powder
定義ChEBI: A hydroxybenzyl alcohol that is phenol substituted by a hydroxymethyl group at C-2.