Key Documents

View All Documentation

158348

4-(Benzyloxy)phenol

Name: 4-(Benzyloxy)phenol
Brand: ALDRICH

98%

Synonym(s):

4-(Phenylmethoxy)phenol, Hydroquinone monobenzyl ether

Select a Size

Change View

About This Item

Linear Formula:

C₆H₅CH₂OC₆H₄OH

CAS Number:

103-16-2

Molecular Weight:

200.23

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24849729

EC Number:

203-083-3

Beilstein/REAXYS Number:

1958305

MDL number:

MFCD00002333

Assay:

98%

Form:

solid

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

100

assay

98%

form

solid

mp

119-120 °C (lit.)

functional group

phenyl

SMILES string

Oc1ccc(OCc2ccccc2)cc1

InChI

1S/C13H12O2/c14-12-6-8-13(9-7-12)15-10-11-4-2-1-3-5-11/h1-9,14H,10H2

InChI key

VYQNWZOUAUKGHI-UHFFFAOYSA-N

Gene Information

human ... TYR(7299)
rat ... Ar(24208)

Description

Application

4-(Benzyloxy)phenol was used in the synthesis of bis(4-benzyloxyphenoxy)phenyl phosphine oxide. It was also used in the preparation of series of hetaryl-azophenol dyes via heterocyclic amines in nitrosyl sulphuric acid.

Still not finding the right product?

Explore all of our products under 4-(Benzyloxy)phenol

pictograms

GHS07

signalword

Warning

hcodes

H317,H319

pcodes

P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis, spectral properties, biological activity and application of new 4-(benzyloxy) phenol derived azo dyes for polyester fiber dyeing.

Yousefi H, et al.

Journal of Molecular Liquids, 180, 51-58 (2013)

Effective melanoma immunotherapy in mice by the skin-depigmenting agent monobenzone and the adjuvants imiquimod and CpG.

Jasper G van den Boorn et al.

PloS one, 5(5), e10626-e10626 (2010-05-26)

Presently melanoma still lacks adequate treatment options for metastatic disease. While melanoma is exceptionally challenging to standard regimens, it is suited for treatment with immunotherapy based on its immunogenicity. Since treatment-related skin depigmentation is considered a favourable prognostic sign during

Retinoic acid synergistically enhances the melanocytotoxic and depigmenting effects of monobenzylether of hydroquinone in black guinea pig skin.

Behrooz Kasraee et al.

Experimental dermatology, 15(7), 509-514 (2006-06-10)

Monobenzylether of hydroquinone (MBEH) has long been utilized for the depigmentation therapy of patients with extensive vitiligo. In this approach, the normally pigmented areas surrounding vitiligo lesions are depigmented to achieve a uniform skin tone. One of the important disadvantages

View All Related Papers

Global Trade Item Number

SKU	GTIN
158348-100G	04061838743855
158348-25G	04061838743862