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525626

Sigma-Aldrich

4-[(N-Boc)aminomethyl]aniline

97%

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About This Item

Linear Formula:
H2NC6H4CH2NHCO2C(CH3)3
CAS Number:
Molecular Weight:
222.28
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

mp

75-78 °C (lit.)

SMILES string

CC(C)(C)OC(=O)NCc1ccc(N)cc1

InChI

1S/C12H18N2O2/c1-12(2,3)16-11(15)14-8-9-4-6-10(13)7-5-9/h4-7H,8,13H2,1-3H3,(H,14,15)

InChI key

UXWQXBSQQHAGMG-UHFFFAOYSA-N

General description

4-[(N-Boc)aminomethyl]aniline is a protected amine.

Application

4-[(N-Boc)aminomethyl]aniline may be used in the synthesis of haptens and 4-(N-boc-aminomethyl)benzene diazonium tetrafluoroborate salt.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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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Covalent modification of carbon nanotubes with anthraquinone by electrochemical grafting and solid phase synthesis.
Ghanem MA, et al.
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Staudinger ligation: a new immobilization strategy for the preparation of small-molecule arrays.
Maja Köhn et al.
Angewandte Chemie (International ed. in English), 42(47), 5830-5834 (2003-12-16)
Sven W Meckelmann et al.
Prostaglandins & other lipid mediators, 130, 8-15 (2017-02-22)
The performance of two derivatization and ionization techniques for the quantitative reversed phase liquid chromatography (LC)- mass spectrometry (MS) analysis of hydroxy fatty acids (OH-PUFA) in plasma was evaluated: One used AMPP (N-(4-aminomethylphenyl)pyridinium chloride) leading to a positive charged amid-derivate
László Szabó et al.
Materials (Basel, Switzerland), 12(1) (2019-01-10)
While intensive efforts are made to prepare carbon fiber reinforced plastics from renewable sources, less emphasis is directed towards elaborating green approaches for carbon fiber surface modification to improve the interfacial adhesion in these composites. In this study, we covalently

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