2-(2-Aminoethyl)-1-methylpyrrolidine - ≥97% , CAS No.51387-90-7

CAS: 51387-90-7 Cat. No.: A102047 Molecular Weight: 128.22 EC Number: 257-169-0

GRADE & PURITY ≥97%

Synonyms

DTXSID401291397 | MFCD00003175 | 2-(1-methyl-pyrrolidin-2-yl)ethylamine | 2-(1-METHYL-PYRROLIDIN-2-YL)-ETHYLAMINE | 2-(1-methylpyrrolidin-2-yl)ethylamine | 2-(1-methylpyrrolidin-2-yl)-ethylamine | [2-(1-methyl-2-pyrrolidinyl)ethyl]amine | 2-(1-Methyl-2-py

Storage

Argon charged,Room temperature

Shipped In

Normal

Overview

Product Description

2-(2-Aminoethyl)-1-methylpyrrolidine labelling acts as probe within microfluidic chip for electrochemiluminescence detection. It acts as electrogenerated chemiluminescence derivatization reagent for carboxylic acid in HPLC.
Product Application

2-(2-Aminoethyl)-1-methylpyrrolidine was used in dual-cloud point extraction and tertiary amine labeling for the quantification of indole-3-acetic acid and indole-3-butyric acid.

Specifications

Synonyms

DTXSID401291397 | MFCD00003175 | 2-(1-methyl-pyrrolidin-2-yl)ethylamine | 2-(1-METHYL-PYRROLIDIN-2-YL)-ETHYLAMINE | 2-(1-methylpyrrolidin-2-yl)ethylamine | 2-(1-methylpyrrolidin-2-yl)-ethylamine | [2-(1-methyl-2-pyrrolidinyl)ethyl]amine | 2-(1-Methyl-2-py

Specifications & Purity

≥97%

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥97%

Names and Identifiers

• Pubchem Sid: 488187121
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488187121
• Canonical Smiles: CN1CCCC1CCN
• IUPAC Name: 2-(1-methylpyrrolidin-2-yl)ethanamine
• InChIKey: PNHGJPJOMCXSKN-UHFFFAOYSA-N
• INCHI: 1S/C7H16N2/c1-9-6-2-3-7(9)4-5-8/h7H,2-6,8H2,1H3
• Isomeric SMILES: CN1CCCC1CCN
• WGK Germany: 2
• UN Number: 2735
• Packing Group: III
• Molecular Weight: 128.22
• Reaxy-Rn: 635820
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635820&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Pyrrolidines
      • Subclass N-alkylpyrrolidines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Pyrrolidines
• Subclass: N-alkylpyrrolidines
• Intermediate Tree Nodes: Not available
• Direct Parent: N-alkylpyrrolidines
• Alternative Parents: Trialkylamines Azacyclic compounds Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: N-alkylpyrrolidine - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as n-alkylpyrrolidines. These are compounds containing a pyrrolidine moiety that is substituted at the N1-position with an alkyl group. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Air Sensitive,Moisture Sensitive
• Refractive Index: 1.4684
• Flash Point(°F): 149 °F
• Flash Point(°C): 65℃
• Molecular Weight: 128.220 g/mol
• XLogP3: 0.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 128.131 Da
• Monoisotopic Mass: 128.131 Da
• Topological Polar Surface Area: 29.300 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 83.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Guimei Zhu, Shihua Long, Hao Sun, Wen Luo, Xia Li, Zaibin Hao.  (2013)  Determination of gibberellins in soybean using tertiary amine labeling and capillary electrophoresis coupled with electrochemiluminescence detection.  JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,      [PMID:24184838] [10.1016/j.jchromb.2013.10.004]