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Dokumente

191558

Sigma-Aldrich

4-Amino-benzylalkohol

98%

Synonym(e):

4-Hydroxymethyl-anilin

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About This Item

Lineare Formel:
H2NC6H4CH2OH
CAS-Nummer:
623-04-1
Molekulargewicht:
123.15
Beilstein:
2078680
EG-Nummer:
210-767-5
MDL-Nummer:
MFCD00014782
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24851494
NACRES:
NA.22

Qualitätsniveau

200

Assay

98%

mp (Schmelzpunkt)

60-65 °C (lit.)

Lagertemp.

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

InChIKey

AXKGIPZJYUNAIW-UHFFFAOYSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

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

Anwendung

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.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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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)
Man Kyu Shim et al.
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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)
The design, synthesis, and initial biological evaluation of a doxorubicin prodrug that contains a dual tumor specific moiety, which allows enhanced tumor recognition potential, is reported. Both a tumor-specific recognition site and a tumor selective enzymatic activation sequence are incorporated
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