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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items N-palmitoylglycine - ≥98% , CAS No.2441-41-0
Synonyms
HY-W074890 | Q27094364 | N-Palmitoyl glycine | PALGLY | BDBM212439 | hexadecanoylglycine | N-hexadecanoyl-glycine | DTXSID40179163 | SCHEMBL515102 | DTXSID2041624 | N-palmitoyl-Gly | CCRIS 3857 | D76997 | Glycine, N-(1-oxohexadecyl)- | N-(1-oxooctadecyl)-
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
HY-W074890 | Q27094364 | N-Palmitoyl glycine | PALGLY | BDBM212439 | hexadecanoylglycine | N-hexadecanoyl-glycine | DTXSID40179163 | SCHEMBL515102 | DTXSID2041624 | N-palmitoyl-Gly | CCRIS 3857 | D76997 | Glycine, N-(1-oxohexadecyl)- | N-(1-oxooctadecyl)-
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
PalGly is an endogenous signaling lipid that modulates calcium influx and nitric oxide production. PalGly inhibits heat-evoked firing of wide dynamic range (WDR) neurons, activates calcium influx in DRG cells and stimulates NO production. Preliminary stud
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Pubchem Sid 488188228 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488188228 Sonrisas canónicas CCCCCCCCCCCCCCCC(=O)NCC(=O)O IUPAC Name 2-(hexadecanoylamino)acetic acid InChIKey KVTFEOAKFFQCCX-UHFFFAOYSA-N INCHI 1S/C18H35NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-17(20)19-16-18(21)22/h2-16H2,1H3,(H,19,20)(H,21,22) Isómeros SMILES CCCCCCCCCCCCCCCC(=O)NCC(=O)O WGK Alemania 2 Peso molecular 313.475 Reaxy-Rn 1798313 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1798313&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic acids and derivatives Clase Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - N-acyl-alpha amino acids and derivatives Direct Parent N-acyl-alpha amino acids Alternative Parents N-acyl amines Secondary carboxylic acid amides Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents N-acyl-alpha-amino acid - Fatty amide - N-acyl-amine - Fatty acyl - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid - Monocarboxylic acid or derivatives - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aliphatic acyclic compound Descripción This compound belongs to the class of organic compounds known as n-acyl-alpha amino acids. These are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. External Descriptors N-acyl amines 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad DMSO: >10 mg/mL Peso molecular 313.500 g/mol XLogP3 6.500 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 16 Exact Mass 313.262 Da Monoisotopic Mass 313.262 Da Topological Polar Surface Area 66.400 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 280.000 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
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