ChemicalBook > CAS DataBase List > Vanillyl alcohol

Vanillyl alcohol

Product Name
Vanillyl alcohol
CAS No.
498-00-0
Chemical Name
Vanillyl alcohol
Synonyms
4-HYDROXY-3-METHOXYBENZYL ALCOHOL;Vanillin alcohol;Vanillinol;VANILLYL ALCOHOL(RG);4-Hydroxy-3-Methoxybenze-neMenthanol;4-HYDROXY-3-METHOXYBENZYL ALCOHOL (VANILLYL ALCOHOL);NSC 3993;vanillol;Vanillyl;FEMA 3737
CBNumber
CB8709532
Molecular Formula
C8H10O3
Formula Weight
154.16
MOL File
498-00-0.mol
More
Less

Vanillyl alcohol Property

Melting point:
110-117 °C (lit.)
Boiling point:
237.52°C (rough estimate)
Density 
1.1690 (rough estimate)
refractive index 
1.4620 (estimate)
FEMA 
3737 | VANILLYL ALCOHOL
storage temp. 
Inert atmosphere,Room Temperature
solubility 
soluble in Methanol
form 
Fine Crystalline Powder
pka
9.75±0.18(Predicted)
color 
Off-white to beige
Odor
at 100.00 %. sweet creamy vanilla caramellic coconut graham cracker tonka milky powdery
Odor Type
creamy
Water Solubility 
Soluble in 95% ethanol (5 %), water, and oils.
JECFA Number
886
BRN 
1910044
Stability:
Stable. Incompatible with strong oxidizing agents, strong acids.
LogP
0.42
CAS DataBase Reference
498-00-0(CAS DataBase Reference)
NIST Chemistry Reference
4-Hydroxy-3-methoxybenzyl alcohol(498-00-0)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29095090
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
W373702
Product name
Vanillyl alcohol
Purity
≥98%, FG
Packaging
100g
Price
$115
Updated
2024/03/01
Sigma-Aldrich
Product number
W373702
Product name
Vanillyl alcohol
Purity
≥98%, FG
Packaging
1kg
Price
$386
Updated
2024/03/01
Sigma-Aldrich
Product number
175536
Product name
4-Hydroxy-3-methoxybenzyl alcohol
Purity
98%
Packaging
50g
Price
$66.8
Updated
2024/03/01
Sigma-Aldrich
Product number
175536
Product name
4-Hydroxy-3-methoxybenzyl alcohol
Purity
98%
Packaging
250g
Price
$145
Updated
2024/03/01
TCI Chemical
Product number
V0018
Product name
Vanillyl Alcohol
Purity
>98.0%(GC)
Packaging
25g
Price
$63
Updated
2024/03/01
More
Less

Vanillyl alcohol Chemical Properties,Usage,Production

Description

4-hydroxy-3-methoxybenzyl alcohol (also known as vanillyl alcohol) is often used as a deodorant component that is active in preventing the formation of body odor. It can also be used as a flavoring agent. Recent studies have also demonstrated that it has certain pharmacological effects. For example, it has been confirmed that it has certain neuro-protective effects through suppressing the oxidative stress and anti-apoptotic activity in toxin-induced dopaminergic MN9D cells, making it a potential candidate for the treatment of neurodegenerative diseases such as Parkinson’s disease.

Chemical Properties

Vanillyl alcohol is a lignin derived aromatic diol. It has a mild, sweet, balsamic, vanilla-like odor.  It has a potential for the production of renewable epoxy thermosets. A bio-based bisphenolic analogue, bisguaiacol, was synthesized via the electrophilic aromatic condensation of vanillyl alcohol and guaiacol. From this, the diglycidyl ether of bisguaiacol was prepared. Further, three single aromatic diglycidyl ethers were synthesized from vanillyl alcohol, gastrodigenin, and hydroquinone. 

Chemical Properties

crystalline white to off-white powder

Uses

Used as a flavoring agent. Other possible uses, vanilla, coconut, cream and other dairy nuances, coumarin.

Definition

ChEBI: Vanillyl alcohol is a monomethoxybenzene that is 2-methoxyphenol substituted by a hydroxymethyl group at position 4. It has a role as a plant metabolite. It is a member of guaiacols and a member of benzyl alcohols.

Taste threshold values

Sweet, creamy and milky with a slightly powdery mouthfeel.

General Description

Vanillyl alcohol belongs to the phenolic group of compounds which are widely used as oxidants in food products.

Biochem/physiol Actions

Odor at 1.0%: sweet creamy, phenolic, vanilla and coconut-like with slight brown and coumarinic nuances.

Synthesis

Vanillyl alcohol is prepared from Vanillin by hydrogenation in presence of Platinum black.

References

Brune, I, et al. "Under the influence of the active deodorant ingredient 4-hydroxy-3-methoxybenzyl alcohol, the skin bacterium Corynebacterium jeikeium moderately responds with differential gene expression." Journal of Biotechnology 127.1(2006):21-33.
Hsu, Lun Chung, Z. H. Wen, and K. Y. Lee. "Use of vanillyl alcohol for the treatment of Parkinson's disease." (2009).
Kim, I. S., D. K. Choi, and H. J. Jung. "Neuroprotective effects of vanillyl alcohol in Gastrodia elata Blume through suppression of oxidative stress and anti-apoptotic activity in toxin-induced dopaminergic MN9D cells." Molecules 16.7(2011):5349.

Vanillyl alcohol Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Vanillyl alcohol Suppliers

HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Target molecule Corp.
Tel
857-239-0968
Fax
857-239-8801
Email
service1@targetmol.com
Country
United States
ProdList
2559
Advantage
60
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32165
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
United States Biological
Tel
--
Fax
--
Email
sales@advtechind.com
Country
United States
ProdList
6075
Advantage
58
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
Ernesto Ventós S.A.
Tel
--
Fax
--
Email
info@ventos.com
Country
United States
ProdList
2257
Advantage
58
Beijing Lys Chemicals Co, LTD.
Tel
--
Fax
--
Email
jiayanyong@lyschem.com
Country
United States
ProdList
710
Advantage
58
WholeChem, LLC
Tel
--
Fax
--
Email
info@wholechem.com
Country
United States
ProdList
814
Advantage
58
Excellentia International
Tel
--
Fax
--
Email
info@excellentiaint.com
Country
United States
ProdList
567
Advantage
58
M&U International LLC
Tel
--
Fax
--
Email
sales@mu-intel.com
Country
United States
ProdList
2011
Advantage
58
Pyrazine Specialties, Inc.
Tel
--
Fax
--
Country
United States
ProdList
1265
Advantage
30
Prodasynth
Tel
--
Fax
--
Email
info@prodasynth.com
Country
United States
ProdList
423
Advantage
58
Qingdao Free Trade Zone United International Co Ltd
Tel
--
Fax
--
Email
info@unitedint.com
Country
United States
ProdList
604
Advantage
58
Lluch Essence S.L.
Tel
--
Fax
--
Email
web@lluche.com
Country
United States
ProdList
2352
Advantage
58
Penta International Corporation
Tel
--
Fax
--
Email
lisaa@pentamfg.com
Country
United States
ProdList
5042
Advantage
58
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
MedChemExpress
Tel
--
Fax
--
Email
sales@medchemexpress.com
Country
United States
ProdList
6398
Advantage
58
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
HBCChem Inc.
Tel
--
Fax
--
Email
sales@hbcchem-inc.com
Country
United States
ProdList
4569
Advantage
30
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60
Chem-Impex International, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6730
Advantage
64
Penta Manufacturing Company
Tel
--
Fax
--
Email
sales@pentamfg.com
Country
United States
ProdList
5076
Advantage
65
Advanced Synthesis Technologies
Tel
--
Fax
--
Email
sales@advancedsynthesis.com
Country
United States
ProdList
4775
Advantage
61
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
United States
ProdList
6814
Advantage
81
INDOFINE Chemical Company, Inc.
Tel
--
Fax
--
Email
chemical@indofinechemical.com
Country
United States
ProdList
6176
Advantage
69
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
City Chemical LLC
Tel
--
Fax
--
Email
sales@citychemical.com
Country
United States
ProdList
6708
Advantage
72
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
Chemiplus Corporation
Tel
--
Fax
--
Email
okazaki@chemiplus.com
Country
United States
ProdList
3198
Advantage
38
Syntech Labs
Tel
--
Fax
--
Email
info@syntechlabs.com
Country
United States
ProdList
730
Advantage
43
Sciencelab.com, Inc.
Tel
--
Fax
--
Email
accounting@sciencelab.com
Country
United States
ProdList
4159
Advantage
82
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
Fontarome Chemical, Inc.
Tel
--
Fax
--
Email
cindy_sonsthagen@fontaromechemical.com
Country
United States
ProdList
268
Advantage
38
MP Biomedicals, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6561
Advantage
81
Pfaltz & Bauer, Inc.
Tel
--
Fax
--
Email
sales@pfaltzandbauer.com
Country
United States
ProdList
6828
Advantage
72
City Chemicals Corporation
Tel
--
Fax
--
Country
United States
ProdList
6460
Advantage
72
ChemPacific Corporation
Tel
--
Fax
--
Email
sales@chempacific.com
Country
United States
ProdList
6891
Advantage
51
ASDI Incorporated
Tel
--
Fax
--
Email
customerservice@asdi.net
Country
United States
ProdList
6922
Advantage
67
More
Less

View Lastest Price from Vanillyl alcohol manufacturers

Hebei Weibang Biotechnology Co., Ltd
Product
Vanillyl alcohol 498-00-0
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100 MT
Release date
2024-11-14
Hebei Weibang Biotechnology Co., Ltd
Product
Vanillyl alcohol 498-00-0
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500000kg
Release date
2024-10-25
Hebei Yanxi Chemical Co., Ltd.
Product
Vanillyl alcohol 498-00-0
Price
US $10.00-1.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
20 tons
Release date
2023-09-28

498-00-0, Vanillyl alcoholRelated Search:


  • 3,4-Dihydroxybenzyl alcohol 3-Methyl ester
  • 4-Hydroxy-3-Methoxybenze-neMenthanol
  • Vanillinol
  • α,4-Dihydroxy-3-Methoxytoluene
  • 2-Hydroxy-5-(hydroxymethyl)anisole, 4-Hydroxy-3-methoxybenzyl alcohol, Vanillyl alcohol
  • 4-Hydroxy-3-Methoxybenzyl alcohol, 99% 50GR
  • 3-Methoxy-4-hydroxybenzyl alcohol
  • Vanillic alcohol
  • Vanillin alcohol
  • 4-HYDROXY-3-METHOXYBENZYL ALCOHOL, 98+%
  • 4-HYDROXY-3-METHOXYBENZYL ALCOHOL (VANILLYL ALCOHOL)
  • 4-Hydroxy-3-methoxybenzyl alcohol,99%
  • VANILLYL ALCOHOL(RG)
  • Hydroxy-3-Methoxybenzyl alc
  • 4-Hydroxy-3-Methoxybenzyl alcohol 98%
  • NSC 3993
  • Vanillin Impurity 3
  • 4-HYDROXY-3-METHOXYBENZYL ALCOHOL
  • 4-hydroxy-3-methoxy-benzenemethano
  • 4-hydroxy-3-methoxybenzyl
  • 4-hydroxy-3-methoxybenzylalcohol(vanillicalcohol)
  • Benzenemethanol, 4-hydroxy-3-methoxy-
  • vanillol
  • RARECHEM AL BD 0101
  • VANILLYL ALCOHOL
  • VANILLYL ALCOHOL MI
  • VANILLYL ALCOHOL 98+%
  • Vanillyl alcohol (4-Hydroxy-3-methoxybenzyl alcohol)
  • Vanillyl
  • FEMA 3737
  • A 4-DIHYDROXY-3-METHOXYTOLUENE
  • CITRONELLOL, D-(SG)
  • HOMOVANILLICALCOHOL
  • 4-HYDROXY-3-METHOXYBENZENEMETHANOL
  • 4-HYDROXYMETHYL-2-METHOXY-PHENOL
  • 4-Hydroxy-3-methoxybenzyl alcohol USP/EP/BP
  • para-vanillyl alcohol
  • 4-Hydroxy-3-Methoxybenzyl Alcohol CAS 498-00-0 C8h10o3
  • TIANFU-CHEM 498-00-0 4-Hydroxy-3-methoxybenzyl alcohol
  • HEXADECYL 2-ETHYLHEXANOATE 59130-69-7
  • Vanillyl alcohol (6CI, 8CI)
  • Vanillyl Alcohol, ≥ 98.0%
  • 498-00-0
  • 4980-00-0
  • 2560-07-7
  • HOC6H3CH2OHOCH3
  • HOC6H3OCH3CH2OH
  • CH3OC6H3OHCH2OH
  • ALCOHOL
  • Oxygen Compounds
  • Organic Building Blocks
  • Building Blocks
  • Alcohols
  • C7 to C8
  • Inhibitors
  • Bifunctional Linkers
  • Linkers and Crosslinkers
  • Alcohols