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191558

Sigma-Aldrich

4-Aminobenzyl alcohol

98%

Synonym(s):

4-(Hydroxymethyl)aniline

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About This Item

Linear Formula:
H2NC6H4CH2OH
CAS Number:
623-04-1
Molecular Weight:
123.15
Beilstein/REAXYS Number:
2078680
EC Number:
210-767-5
MDL number:
MFCD00014782
UNSPSC Code:
12352100
PubChem Substance ID:
24851494
NACRES:
NA.22

Quality Level

200

assay

98%

mp

60-65 °C (lit.)

storage temp.

2-8°C

SMILES string

Nc1ccc(CO)cc1

InChI

1S/C7H9NO/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5,8H2

InChI key

AXKGIPZJYUNAIW-UHFFFAOYSA-N

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General description

4-Aminobenzyl alcohol is used as a starting material to synthesize other organic compounds.

Application

4-Aminobenzyl alcohol can be used:
  • In the synthesis of 4-{N-[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutylamino}benzyl ester.
  • As a reactant to synthesize cross-azo compounds and cathepsin B cleavable dipeptide linker.
  • As a starting material to synthesize hydrogelators for drug delivery applications.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG9235
BCCG0127
0000082951
BCBZ3926
BCCB0744

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Katarzyna Gorska et al.
Chemical communications (Cambridge, England), 47(15), 4364-4366 (2011-03-04)
Nucleic acid templated reactions have attracted significant attention for nucleic acid sensing. Herein we report a general design which extends the potential of nucleic acid templated reactions to unleash the function of a broad diversity of small molecules such as
A novel 4-aminobenzyl ester-based carboxy-protecting group for synthesis of atypical peptides by Fmoc-But solid-phase chemistry.
Chan WC, et al.
Journal of the Chemical Society. Chemical Communications, 21, 2209-2210 (1995)
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C Elvira et al.
Biomaterials, 23(9), 1955-1966 (2002-05-09)
The design and preparation of novel biodegradable hydrogels developed by the free radical polymerization of acrylamide and acrylic acid, and some formulations with bis-acrylamide, in the presence of a corn starch/ethylene-co-vinyl alcohol copolymer blend (SEVA-C), is reported. The redox system
Franciscus M H de Groot et al.
Molecular cancer therapeutics, 1(11), 901-911 (2002-12-17)
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