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A65204

Sigma-Aldrich

2-Picolylamine

99%

Synonym(s):

2-(Aminomethyl)pyridine

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CN¥546.80
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5 G
CN¥233.94
25 G
CN¥546.80
100 G
CN¥1,480.93

About This Item

Empirical Formula (Hill Notation):
C6H8N2
CAS Number:
3731-51-9
Molecular Weight:
108.14
Beilstein:
108054
EC Number:
223-090-5
MDL number:
MFCD00006360
UNSPSC Code:
12352100
PubChem Substance ID:
24891101
NACRES:
NA.22

CN¥233.94

Please contact Customer Service for Availability
Request a Bulk Order

Quality Level

100

Assay

99%

form

liquid

refractive index

n20/D 1.544 (lit.)

bp

82-85 °C/12 mmHg (lit.)

density

1.049 g/mL at 25 °C (lit.)

SMILES string

NCc1ccccn1

InChI

1S/C6H8N2/c7-5-6-3-1-2-4-8-6/h1-4H,5,7H2

InChI key

WOXFMYVTSLAQMO-UHFFFAOYSA-N

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Show Differences

1 of 4

This Item
H56800P62003H57009
2-Picolylamine 99%

A65204

2-Picolylamine

2-Hydroxypyridine 97%

H56800

2-Hydroxypyridine

2-Pyridinecarboxaldehyde 99%

P62003

2-Pyridinecarboxaldehyde

3-Hydroxypyridine 98%

H57009

3-Hydroxypyridine

assay

99%

assay

97%

assay

99%

assay

98%

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

200

density

1.049 g/mL at 25 °C (lit.)

density

-

density

1.126 g/mL at 25 °C (lit.)

density

-

bp

82-85 °C/12 mmHg (lit.)

bp

280-281 °C (lit.)

bp

181 °C (lit.)

bp

-

refractive index

n20/D 1.544 (lit.)

refractive index

-

refractive index

n20/D 1.536 (lit.)

refractive index

-

form

liquid

form

-

form

-

form

-

Application

2-Picolylamine is a bihaptic amine[1] that can be used:
  • As a key precursor to synthesize various ionic liquids through the formation of β-amino alcohols as intermediates.[1]
  • As a chelating ligand for the synthesis of complexes such as zinc picolylamine complex[2] and Cu(II) picolylamine complex.[3]
  • To functionalize poly(styrene-co-maleic anhydride) (PSMA) resin to facilitate the adsorption of uranium from aqueous solution.[4]

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
  • Specification Sheet

    • Choose from one of the most recent versions:

    Certificates of Analysis (COA)

    Lot/Batch Number
    SDBB1105
    0000242641
    0000221434
    0000221411
    0000184226

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    Glycosylated metal chelators as anti-parasitic agents with tunable selectivity.
    Reddy A, et al.
    Dalton Transactions, 46(16), 5297-5307 (2017)
    Cengiz Yenikaya et al.
    Bioorganic & medicinal chemistry, 18(2), 930-938 (2009-12-17)
    A novel proton transfer compound, pyridin-2-ylmethanaminium 2,4-dichloro-5-sulfamoylbenzoate (1), and a mixed-ligand Zn(II) complex, bis(2,4-dichloro-5-sulfamoylbenzoate)(2-aminomethylpyridine)aquazinc(II) monohydrate (2), have been synthesized from the same free ligands, which are 2,4-dichloro-5-sulfamoylbenzoic acid (Hsba) and 2-aminomethylpyridine (amp). They have been characterized by elemental, spectral ((1)H
    Recovery of uranium (VI) from aqueous solution by 2-picolylamine functionalized poly (styrene-co-maleic anhydride) resin.
    Liu S, et al.
    Journal of Colloid and Interface Science, 497(16), 385-392 (2017)
    Structure of tris(2-picolylamine) zinc (II) dichloride-ethanol,[Zn (α-pic)3] Cl2.EtOH; a complex related to an FeII spin crossover complex.
    Mikami-Kido M and Saito Y
    Acta Crystallographica Section B, Structural Crystallography and Crystal Chemistry, 38(2), 452-455 (1982)
    Solvent-free Al(OTf)3-catalyzed aminolysis of 1, 2-epoxides by 2-picolylamine: a key step in the synthesis of ionic liquids.
    Fringuelli F, et al.
    The Journal of Organic Chemistry, 69(22), 7745-7747 (2004)
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