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513261

Sigma-Aldrich

2,3,5-Collidine

99%

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Synonym(s):
2,3,5-Trimethylpyridine
Empirical Formula (Hill Notation):
C8H11N
CAS Number:
Molecular Weight:
121.18
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

refractive index

n20/D 1.508 (lit.)

bp

184 °C (lit.)

density

0.931 g/mL at 25 °C (lit.)

SMILES string

Cc1cnc(C)c(C)c1

InChI

1S/C8H11N/c1-6-4-7(2)8(3)9-5-6/h4-5H,1-3H3

InChI key

GFYHSKONPJXCDE-UHFFFAOYSA-N

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

165.0 °F

Flash Point(C)

73.9 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Influence of alkylpyridine additives in electrolyte solution on the performance of dye-sensitized solar cell.
Kusama H, et al.
Solar Energy Mat. and Solar Cells, 80(2), 167-179 (2003)
Rapid in vivo fingerprinting of nonvolatile compounds in breath by extractive electrospray ionization quadrupole time-of-flight mass spectrometry.
Huanwen Chen et al.
Angewandte Chemie (International ed. in English), 46(4), 580-583 (2006-11-03)
Hydrothermal in situ ligand reaction: copper (II)-mediated stepwise oxidation of 2, 3, 5-and 2, 4, 6-trimethylpyridine to pyridinecarboxylates.
Li CJ, et al.
CrystEngComm, 12(2), 425-433 (2010)
Alan J Cameron et al.
Chemistry, an Asian journal, 12(24), 3195-3202 (2017-11-04)
Herein we report the unique conformations adopted by linear and cyclic tetrapeptides (CTPs) containing 2-aminobenzoic acid (2-Abz) in solution and as single crystals. The crystal structure of the linear tetrapeptide H
Jonita Stankevičiūtė et al.
Scientific reports, 6, 39129-39129 (2016-12-17)
Pyridinols and pyridinamines are important intermediates with many applications in chemical industry. The pyridine derivatives are in great demand as synthons for pharmaceutical products. Moreover, pyridines are used either as biologically active substances or as building blocks for polymers with

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