N-(2-Hydroxyethyl)dodecanamide - ≥98% , CAS No.142-78-9

CAS: 142-78-9 Cat. No.: N190895 Molecular Weight: 243.39 EC Number: 205-560-1

GRADE & PURITY ≥98%

Synonyms

Lauridit LM | Lauryl ethanolamide | LMFA08040041 | 098P2IGT76 | Crillon L.M.E. | Dodecylethanol amide | EINECS 205-560-1 | Incromide LCL | Lauramide MEA | N-(2-Hydroxyethyl)dodecaneamide | Lauric acid ethanolamide | Lauroyl monoethanolamide | FT-0625582 |

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Synonyms

Lauridit LM | Lauryl ethanolamide | LMFA08040041 | 098P2IGT76 | Crillon L.M.E. | Dodecylethanol amide | EINECS 205-560-1 | Incromide LCL | Lauramide MEA | N-(2-Hydroxyethyl)dodecaneamide | Lauric acid ethanolamide | Lauroyl monoethanolamide | FT-0625582 |

Specifications & Purity

≥98%

Storage

Store at 2-8°C

Shipped In

Wet ice

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

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 504751759
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751759
• Canonical Smiles: CCCCCCCCCCCC(=O)NCCO
• IUPAC Name: N-(2-hydroxyethyl)dodecanamide
• InChIKey: QZXSMBBFBXPQHI-UHFFFAOYSA-N
• INCHI: 1S/C14H29NO2/c1-2-3-4-5-6-7-8-9-10-11-14(17)15-12-13-16/h16H,2-13H2,1H3,(H,15,17)
• Isomeric SMILES: CCCCCCCCCCCC(=O)NCCO
• Molecular Weight: 243.39
• Reaxy-Rn: 510552
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=510552&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboximidic acids and derivatives
      • Subclass Carboximidic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboximidic acids and derivatives
• Subclass: Carboximidic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboximidic acids
• Alternative Parents: Propargyl-type 1,3-dipolar organic compounds Alkanolamines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidic acid - Alkanolamine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as carboximidic acids. These are organic acids with the general formula RC(=N)-OH (R=H, organic group).
• External Descriptors: N-acyl ethanolamines (endocannabinoids)

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

Associated Targets(Human)

DGAT1 Tclin Diacylglycerol O-acyltransferase 1 (1719 Activities)

Discover Target: DGAT1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Melt Point(°C): 88-89℃
• Molecular Weight: 243.390 g/mol
• XLogP3: 4.000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 12
• Exact Mass: 243.22 Da
• Monoisotopic Mass: 243.22 Da
• Topological Polar Surface Area: 49.300 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 172.000
• 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