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Quality Level
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Find documentation for the products that you have recently purchased in the Document Library.
A novel 4-aminobenzyl ester-based carboxy-protecting group for synthesis of atypical peptides by Fmoc-But solid-phase chemistry.
Journal of the Chemical Society. Chemical Communications, 21, 2209-2210 (1995)
The rational design of a peptide-based hydrogel responsive to H 2 S
Chemical Communications (Cambridge, England), 51(97), 17273-17276 (2015)
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
Selective Single-Step Oxidation of Amine to Cross-Azo Compounds with an Unhampered Primary Benzyl Alcohol Functionality
Organic Letters, 20(21), 6725-6729 (2018)
Supramolecular hydrogels for enzymatically triggered self-immolative drug delivery
Tetrahedron, 66(14), 2614-2618 (2010)
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