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127809

Sigma-Aldrich

4-Methylbenzylalkohol

98%

Synonym(e):

(4-Methylphenyl)methanol, (4-Tolyl)methanol, 4-Methylbenzenemethanol, p-Methylbenzyl alcohol, p-Tolualcohol, p-Tolylcarbinol, p-Tolylmethanol

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About This Item

Lineare Formel:
CH3C6H4CH2OH
CAS-Nummer:
589-18-4
Molekulargewicht:
122.16
EG-Nummer:
209-639-1
MDL-Nummer:
MFCD00004664
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24847799
NACRES:
NA.22

Qualitätsniveau

100

Assay

98%

bp

217 °C (lit.)

mp (Schmelzpunkt)

59-61 °C (lit.)

Funktionelle Gruppe

hydroxyl

SMILES String

Cc1ccc(CO)cc1

InChI

1S/C8H10O/c1-7-2-4-8(6-9)5-3-7/h2-5,9H,6H2,1H3

InChIKey

KMTDMTZBNYGUNX-UHFFFAOYSA-N

Verwandte Kategorien

Allgemeine Beschreibung

4-Methylbenzyl alcohol is widely used in flavoring and fragrances. Used as a precursor to synthesize aldehydes and polycarbonates.

Anwendung

4-Methylbenzyl alcohol was used in the preparation of polycarbonates. It was also used to synthesize alcohols.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H319

Gefahreneinstufungen

Eye Irrit. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
STBK3184
STBH6928
STBH3603
STBG0114V
STBF4095V

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Sigma-Aldrich

510556

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Sigma-Aldrich

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Hironao Sajiki et al.
Chemical & pharmaceutical bulletin, 51(3), 320-324 (2003-03-04)
Employment of a Pd/C-pyridine combination as a catalyst is a very useful method for the selective removal (hydrogenolysis) of phenolic O-benzyl, N-Cbz and benzyl ester protective groups and for the selective hydrogenation of nitro and olefin functions of phenol derivatives
Koichiro Mikami et al.
Journal of the American Chemical Society, 135(18), 6826-6829 (2013-05-01)
An organocatalyzed ring-opening polymerization methodology was developed for the preparation of polycarbonates derived from glucose as a natural product starting material. The cyclic 4,6-carbonate monomer of glucose having the 1, 2, and 3 positions methyl-protected was prepared in three steps
Bryce V Plapp et al.
Archives of biochemistry and biophysics, 701, 108825-108825 (2021-03-07)
Enzymes typically have high specificity for their substrates, but the structures of substrates and products differ, and multiple modes of binding are observed. In this study, high resolution X-ray crystallography of complexes with NADH and alcohols show alternative modes of
Carla Villa et al.
International journal of cosmetic science, 30(2), 139-144 (2008-04-02)
Several alcohols--interesting as cosmetic fragrances whose main preparative route on an industrial scale or in the research laboratory is the reduction of the corresponding carbonyl compound--were obtained by a solvent-free methodology in a green chemistry context. The process involves the
B J Day et al.
Research communications in chemical pathology and pharmacology, 76(1), 117-120 (1992-04-01)
Pulmonary metabolites of p-xylene, p-methylbenzyl alcohol (PMBA) and 2,5-dimethylphenol (DMP), were employed to investigate the divergent effects of p-xylene on pulmonary and hepatic metabolism. Rats were given PMBA, DMP, or 10% cremophore (control) ip daily for 3 days, and effects
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Global Trade Item Number

SKUGTIN
127809-100G4061832879840
127809-25G4061838725196
127809-5G4061838725202

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