Skip to Content
Merck
All Photos(1)

Documents

T58009

Sigma-Aldrich

Tridecylamine

98%

Synonym(s):

1-Aminotridecane

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3(CH2)12NH2
CAS Number:
Molecular Weight:
199.38
Beilstein:
1739990
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

bp

265 °C (lit.)

mp

30-32 °C (lit.)

SMILES string

CCCCCCCCCCCCCN

InChI

1S/C13H29N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14/h2-14H2,1H3

InChI key

ABVVEAHYODGCLZ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Tridecylamine can undergo:
  • Dehydrogenation to nitriles catalyzed by ruthenium complex.
  • Aerobic oxidation to carbonyl compounds catalyzed by vitamin C and Cu complex.

Tridecylamine is generally used in introducing C13 chain to the substrate. Some of the application are:
  • Synthesis of alkylated 1,2,4-triazoles as bridging ligand in the preparation of polymeric 1-dimensional chains of iron(II) species.
  • Synthesis of amphiphiles such as N-tridecyl-β-hydroxypropionic acid amide (THPA) and N-(β-hydroxyethyl)tridecanoic acid amide (HETA).
  • As a ligand in the preparation of palladium-based catalyst, [PdCl2(TDA)2].

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

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’.

Already Own This Product?

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

Visit the Document Library

Catalytic investigation of PdCl2 (TDA)2 immobilized on hydrophobic graphite oxide in the hydrogenation of 1-pentyne and the Heck coupling reaction.
Mastalir A, et al.
Reaction Kinetics, Mechanisms and Catalysis, 113(1), 61-68 (2014)
1-Heptyne semihydrogenation catalized by palladium or rhodium complexes: Influence of: metal atom, ligands and the homo/heterogeneous condition.
Quiroga M E, et al.
Applied Catalysis A: General, 326(2), 121-129 (2007)
Effect of the exchange of substituent position in an amide amphiphile on the monolayer characteristics.
Vollhardt D and Wagner R
The Journal of Physical Chemistry B, 110(30), 14881-14889 (2006)
Spin-transition behaviour in chains of Fe II bridged by 4-substituted 1, 2, 4-triazoles carrying alkyl tails,.
Roubeau O, et al.
New. J. Chem., 25(1), 144-150 (2001)
Copper/ascorbic acid dyad as a catalytic system for selective aerobic oxidation of amines
Srogl J and Voltrova S
Organic Letters, 11(4), 843-845 (2009)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service