Arachidic acid N-hydroxysuccinimide ester - ≥95% , CAS No.69888-87-5

CAS: 69888-87-5 Cat. No.: A353276 Molecular Weight: 409.6

GRADE & PURITY ≥95%

Synonyms

(2,5-dioxopyrrolidin-1-yl) Icosanoate | 2,5-Dioxopyrrolidin-1-yl icosanoate | F77910 | DTXSID601292084 | 2,5-Dioxo-1-pyrrolidinyl eicosanoate | N-(EICOSANOYLOXY)SUCCINIMIDE | eicosanoic acid n-hydroxysuccinimide ester | BP-29802 | Arachidic Acid N-Hydroxy

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Application

228,229

Overview

Product Application:

N-Hydroxysuccinimide Conjugated Ester derivative of Arachidic Acid , a saturated fatty acid and a minor constituent of peanut oil, coconut oil and corn oil.

Specifications

Synonyms

(2, 5-dioxopyrrolidin-1-yl) Icosanoate | 2, 5-Dioxopyrrolidin-1-yl icosanoate | F77910 | DTXSID601292084 | 2, 5-Dioxo-1-pyrrolidinyl eicosanoate | N-(EICOSANOYLOXY)SUCCINIMIDE | eicosanoic acid n-hydroxysuccinimide ester | BP-29802 | Arachidic Acid N-Hydroxy

Specifications & Purity

≥95%

Storage

Store at -20°C, Argon charged

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥95%

Names and Identifiers

• Pubchem Sid: 488197041
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488197041
• Canonical Smiles: CCCCCCCCCCCCCCCCCCCC(=O)ON1C(=O)CCC1=O
• IUPAC Name: (2,5-dioxopyrrolidin-1-yl) icosanoate
• InChIKey: NWQWMRGPQVJCNH-UHFFFAOYSA-N
• INCHI: 1S/C24H43NO4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-24(28)29-25-22(26)20-21-23(25)27/h2-21H2,1H3
• Isomeric SMILES: CCCCCCCCCCCCCCCCCCCC(=O)ON1C(=O)CCC1=O
• Molecular Weight: 409.6
• Reaxy-Rn: 1551563
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1551563&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Pyrrolidines
      • Subclass Pyrrolidones

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Pyrrolidines
• Subclass: Pyrrolidones
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyrrolidine-2-ones
• Alternative Parents: Dicarboximides Lactams Monocarboxylic acids and derivatives Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: 2-pyrrolidone - Dicarboximide - Lactam - Azacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as pyrrolidine-2-ones. These are pyrrolidines which bear a C=O group at position 2 of the pyrrolidine ring.
• 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: Moisture sensitive
• Melt Point(°C): 95-97°C
• Molecular Weight: 409.600 g/mol
• XLogP3: 8.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 20
• Exact Mass: 409.319 Da
• Monoisotopic Mass: 409.319 Da
• Topological Polar Surface Area: 63.700 Ų
• Heavy Atom Count: 29
• Formal Charge: 0
• Complexity: 448.000
• 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