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W373702

Sigma-Aldrich

Vanillyl alcohol

≥98%, FG

Synonym(s):

4-Hydroxy-3-methoxybenzyl alcohol, NSC 3993, Vanillyl alcohol

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About This Item

Linear Formula:
HOC6H3(OCH3)CH2OH
CAS Number:
498-00-0
Molecular Weight:
154.16
FEMA Number:
3737
Beilstein:
1910044
EC Number:
207-852-4
Council of Europe no.:
690
MDL number:
MFCD00004659
UNSPSC Code:
12164502
PubChem Substance ID:
24901864
Flavis number:
2.213
NACRES:
NA.21

biological source

synthetic

Quality Level

400

grade

FG
Kosher

Agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002

description

Natural occurrence: Beer

Assay

≥98%

mp

110-117 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

creamy; sweet; vanilla

SMILES string

COc1cc(CO)ccc1O

InChI

1S/C8H10O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-4,9-10H,5H2,1H3

InChI key

ZENOXNGFMSCLLL-UHFFFAOYSA-N

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Application

Possible uses: vanilla, coconut, cream and other dairy nuances, coumarin notes.

Biochem/physiol Actions

Odor at 1.0%: sweet creamy, phenolic, vanilla and coconut-like with slight brown and coumarinic nuances.
Taste at 50 ppm: creamy waxy, sweet milky, powdery with an ice cream-like nuance.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBS1123
SHBR7574
SHBQ0421
SHBP4485
SHBN7425

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Mosciano, Gerard
Perfumer & Flavorist, 34, 51-51 (2009)
Padmesh Venkitasubramanian et al.
The Journal of biological chemistry, 282(1), 478-485 (2006-11-15)
Aldehyde oxidoreductase (carboxylic acid reductase (Car)) catalyzes the magnesium-, ATP-, and NADPH-dependent reduction of carboxylic acids to their corresponding aldehydes. Heterologous expression of the car gene in Escherichia coli afforded purified recombinant enzyme with a specific activity nearly 50-fold lower
Kiki L Larsen et al.
The journal of physical chemistry. B, 115(39), 11470-11480 (2011-08-13)
Structural analysis of plant materials, i.e., lignin, cellulose, hemicellulose, etc., supports the growing interest of their uses, e.g., as sources for biofuels or materials. Lignin is a main polymer formed from three phenolic presursors, containing none, one, or two OMe
In Su Kim et al.
Molecules (Basel, Switzerland), 16(7), 5349-5361 (2011-06-28)
Gastrodia elata Blume (GE) has long been used in oriental countries as a traditional herbal medicine to relieve symptoms associated with neurological ailments such as vertigo, general paralysis and epilepsy. In this study, we have investigated the effects of GE
Claudia Crestini et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 9(21), 5371-5378 (2003-11-13)
In an effort to elucidate the role of phenolic and non-phenolic lignin subunits in a laccase mediator (LM) system, vanillyl alcohol was oxidized with laccase in the presence and absence of the mediator 1-hydroxybenzotriazol (HBT). Furthermore, the role of phenolic
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