166952
2-Hydroxybenzyl alcohol
99%
Sinonimo/i:
Salicyl alcohol, Saligenin
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About This Item
Formula condensata:
HOC6H4CH2OH
Numero CAS:
Peso molecolare:
124.14
Beilstein:
1907195
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
99%
Stato
solid
Punto di fusione
83-85 °C (lit.)
Solubilità
ethanol: soluble 5%, clear to very slightly hazy, colorless to light yellow
Gruppo funzionale
hydroxyl
Stringa SMILE
OCc1ccccc1O
InChI
1S/C7H8O2/c8-5-6-3-1-2-4-7(6)9/h1-4,8-9H,5H2
CQRYARSYNCAZFO-UHFFFAOYSA-N
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Categorie correlate
Descrizione generale
2-Hydroxybenzyl alcohol participates in the selective ring opening reaction of 4H-1,3,2-benzodioxasilines.
2-Hydroxybenzyl alcohol can be used as a coupling reagent to synthesize O-heterocycles.
2-Hydroxybenzyl alcohol can be used as a coupling reagent to synthesize O-heterocycles.
Applicazioni
2-Hydroxybenzyl alcohol was used in gastrodin production via biotransformation by cultured cells of Aspergillus foetidus and Penicillium cyclopium.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
Selective ring opening of 4H-1, 3, 2-benzodioxasiline twin monomers.
Kempe P, et al.
New. J. Chem., 35(12), 2735-2739 (2011)
Linlin Fan et al.
Applied biochemistry and biotechnology, 170(1), 138-148 (2013-03-14)
The objective of this work was to take advantage of the resting cells of suitable fungus as an in vitro model to prepare gastrodin from p-2-hydroxybenzyl alcohol (HBA), which mainly exists in the metabolites of the plant Gastrodia elata Blume.
Per Borgquist et al.
Journal of controlled release : official journal of the Controlled Release Society, 113(3), 216-225 (2006-06-27)
A model for simulating the drug release from a swelling and dissolving polymer tablet is presented and verified to data. The model is based on a mechanistic approach, and it can therefore be employed to study the sensitivity of true
Mariagrazia Marucci et al.
Journal of controlled release : official journal of the Controlled Release Society, 114(3), 369-380 (2006-08-15)
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The Journal of biological chemistry, 283(28), 19219-19228 (2008-05-17)
Salicyl alcohol oxidase is an extracellular enzyme that occurs in glandular reservoirs of chrysomelid leaf beetle larvae and catalyzes the formation of salicylaldehyde, a volatile deterrent used by the larvae against predators. Salicyl alcohol is the hydrolysis product of salicin
Global Trade Item Number
SKU | GTIN |
---|---|
166952-100G | 4061838749215 |
166952-25G | 4061838749222 |
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