Choline chloride - 10mM in DMSO , CAS No.67-48-1

CAS: 67-48-1 Cat. No.: C425396 Formule: C₅H₁₄ClNO Poids moléculaire: 139.62 Beilstein Registry Number: 3563126 Numéro CE: 200-655-4

QUALITÉ & PURETÉ 10mM in DMSO

Synonyms

2-Hydroxy-N,N,N-trimethylethanaminium chloride | Cloruro de colina | 2-Hydroxy-N,N,N,-trimethylethanaminium chloride | CHOLINE-D13 CHLORIDE | FT-0665025 | Hormocline | CHOLINE CHLORIDE [VANDF] | F8889-3032 | HMS1922E20 | SR-01000075745 | CHEBI:133341 | DT

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Vue d’ensemble

Choline Chloride is an acyl group acceptor and choline acetyltransferase substrate.
An acyl group acceptor

application：

Choline chloride helps in providing nourishment for pig feed and poultry feed. It acts as a food flavor enhancer. It is used as a precursor of acetylcholine and is a methyl donor in various metabolic processes and in lipid metabolism.

product description：

Choline chloride is the synthetic form of vitamin B4, choline and is a common poultry feed.

Spécifications

Synonymes

2-Hydroxy-N,N,N-trimethylethanaminium chloride | Cloruro de colina | 2-Hydroxy-N,N,N,-trimethylethanaminium chloride | CHOLINE-D13 CHLORIDE | FT-0665025 | Hormocline | CHOLINE CHLORIDE [VANDF] | F8889-3032 | HMS1922E20 | SR-01000075745 | CHEBI:133341 | DT

Spécifications et pureté

10mM in DMSO

Mécanismes biochimiques et physiologiques

Acyl group acceptor and choline acetyltransferase substrate. Important as a precursor of acetylcholine, as a methyl donor in various metabolic processes, and in lipid metabolism. Used as an additive in animal food.

Conditions de stockage de stockage

Store at -80°C

Expédié en

Dry ice packs + Cold packs

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Noms et identifiants

Pubchem Sid

528772638

Sourires canoniques

C[N+](C)(C)CCO.[Cl-]

IUPAC Name

2-hydroxyethyl(trimethyl)azanium;chloride

InChIKey

SGMZJAMFUVOLNK-UHFFFAOYSA-M

INCHI

1S/C5H14NO.ClH/c1-6(2,3)4-5-7;/h7H,4-5H2,1-3H3;1H/q+1;/p-1

Isomères SMILES

C[N+](C)(C)CCO.[Cl-]

WGK Allemagne

1

RTECS

KH2975000

Poids moléculaire

139.62

Beilstein

3563126

Reaxy-Rn

3563126

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3563126&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Classe Organonitrogen compounds
      • Subclass Quaternary ammonium salts

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Quaternary ammonium salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Cholines
• Alternative Parents: Tetraalkylammonium salts 1,2-aminoalcohols Primary alcohols Organopnictogen compounds Organic zwitterions Organic chloride salts Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Choline - Tetraalkylammonium salt - 1,2-aminoalcohol - Alkanolamine - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic chloride salt - Organic salt - Organic zwitterion - Primary alcohol - Organooxygen compound - Amine - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as cholines. These are organic compounds containing a N,N,N-trimethylethanolammonium cation.
• External Descriptors: chloride salt - quaternary ammonium salt

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

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PDE5A Tclin Phosphodiesterase 5A (5113 Activities)

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CA2 Tclin Carbonic anhydrase II (17698 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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HMGCR Tclin HMG-CoA reductase (2475 Activities)

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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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INSR Tclin Insulin receptor (5558 Activities)

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PGR Tclin Progesterone receptor (8562 Activities)

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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: moisture sensitive
• Point de fusion (°C): 302-305°C
• Poids moléculaire: 139.620 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 139.076 Da
• Monoisotopic Mass: 139.076 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 46.500
• 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: 2

XLogP3