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Documenti fondamentali

166952

Sigma-Aldrich

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

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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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.

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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Certificati d'analisi (COA)

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Sigma-Aldrich

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Supelco

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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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Carmen Michalski et al.
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

SKUGTIN
166952-100G4061838749215
166952-25G4061838749222

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