4-Methylpiperidine - suitable for peptide synthesis, 20 % (w/w) in DMF , CAS No.626-58-4

CAS: 626-58-4 Cat. No.: M433148 Formule: C₆H₁₃N Poids moléculaire: 99.18 Beilstein Registry Number: 1083 Numéro CE: 210-954-1

GRADE & PURITY Suitable for peptide synthesis, 20 % (w/w) in DMF

Synonyms

4-methylpyperidine | 4-methyl piperidine | 4-Pipecoline | NSC 66495 | Q-101897 | 4-(methyl)piperidine | DTXSID8060820 | Piperidine, 4-methyl- | 4-Methylpiperidine, glass distilled | J-512924 | 1219798-85-2 | FT-0619420 | P0445 | PS-9331 | EV6HN6HDP8 | gam

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Vue d’ensemble

Application

4-Methylpiperidine solution (20 % in DMF) can be used: In the deprotection of F-moc protecting group which is attached to free amine. In the determination of resin-bound amino acid by UV-Fmoc-quantitation.

Specifications

Synonymes

4-methylpyperidine | 4-methyl piperidine | 4-Pipecoline | NSC 66495 | Q-101897 | 4-(methyl)piperidine | DTXSID8060820 | Piperidine, 4-methyl- | 4-Methylpiperidine, glass distilled | J-512924 | 1219798-85-2 | FT-0619420 | P0445 | PS-9331 | EV6HN6HDP8 | gam

Spécifications et pureté

suitable for peptide synthesis, 20 % (w/w) in DMF

Conditions de stockage de stockage

Room temperature,Argon charged

Expédié en

FedEx DG Service

Grade

Suitable for peptide synthesis

Noms et identifiants

• Sourires canoniques: CC1CCNCC1
• IUPAC Name: 4-methylpiperidine
• InChIKey: UZOFELREXGAFOI-UHFFFAOYSA-N
• INCHI: 1S/C6H13N/c1-6-2-4-7-5-3-6/h6-7H,2-5H2,1H3
• Isomères SMILES: CC1CCNCC1
• WGK Allemagne: 3
• Poids moléculaire: 99.18
• Beilstein: 1083
• Reaxy-Rn: 1083
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1083&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Piperidines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Piperidines
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Piperidines
• Alternative Parents: Dialkylamines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Piperidine - Azacycle - Secondary amine - Secondary aliphatic amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as piperidines. These are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five 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

Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: Moisture sensitive
• Indice de réfraction: n20/D 1.446
• Point d'éclair (°F): 55.4 °F
• Point d'éclair (°C): 9°C
• Point d'ébullition (°C): 124 °C
• Poids moléculaire: 99.170 g/mol
• XLogP3: 1.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 99.1048 Da
• Monoisotopic Mass: 99.1048 Da
• Topological Polar Surface Area: 12.000 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 46.100
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Références

1. Junwu Wei, Yangyang Qian, Lijun Bao, Wenjie Song, Yunmei Bi.  (2024)  Disulfide bonds as a molecular switch of enzyme-activatable anticancer drug precise release for fluorescence imaging and enhancing tumor therapy.  TALANTA,      [PMID:38924984] [10.1016/j.talanta.2024.126394]

2. Yahui Liu, Quan Li, Yanhong Ji, Mohammad Younas, Benqiao He.  (2024)  Preparation of polyaniline conductive membranes through immersion of dopant solution for dye/salt separation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.127531]

3. Tiantian Wei, Jingjing Wu, Xiran Shen, Zhifeng Qiu, Li Guo.  (2021)  Self-Assembled Membrane-like Nanomaterials from Sequence-Defined Peptoid Block Copolymers.  Polymers,  13  (15): (2389).  [PMID:34371992] [10.3390/polym13152389]

4. Hua Weiwen, Wang Yuanguang, Guo Cun-Yue, Wang Jianjun, Li Songjun, Guo Li.  (2020)  Ice Recrystallization Inhibition Activity of Protein Mimetic Peptoids.  Journal of Inorganic and Organometallic Polymers and Materials,  31  (1): (203-208).  [PMID:] [10.1007/s10904-020-01673-9]