C7527

Cloruro de colina

BioReagent, suitable for cell culture, suitable for insect cell culture, ≥98%

• Sinónimos: Cloruro de (2-hidroxietil)trimetilamonio
• Fórmula lineal: (CH₃)₃N(Cl)CH₂CH₂OH
• Número de CAS: 67-48-1
• Peso molecular: 139.62
• Beilstein: 3563126
• Número CE: 200-655-4
• Número MDL: MFCD00011721
• Código UNSPSC: 12352205
• ID de la sustancia en PubChem: 24892968
• NACRES: NA.75

Propiedades

• origen biológico: synthetic (organic)
• Línea del producto: BioReagent
• Ensayo: ≥98%
• Formulario: crystals
• mol peso: M_w 139.62 g/mol
• técnicas: cell culture | insect: suitable; cell culture | mammalian: suitable; cell culture | plant: suitable
• color: white
• pH: 5.0-6.5 (25 °C, 140 g/L)
• mp: 302-305 °C (dec.) (lit.)
• solubilidad: H₂O: 50 mg/mL
• cadena SMILES: [Cl-].C[N+](C)(C)CCO
• InChI: 1S/C5H14NO.ClH/c1-6(2,3)4-5-7;/h7H,4-5H2,1-3H3;1H/q+1;/p-1
• Clave InChI: SGMZJAMFUVOLNK-UHFFFAOYSA-M

Descripción

Descripción general

Choline chloride is a quaternary ammonium salt and associates with hydrogen bond donors (HBD).[1] It is essential for the vital physiological functions and is used as a nutritional additive. Choline is a source of methyl groups for methyl-transfer reactions.[2]

Aplicación

Choline chloride has been used:

• as a component of choline acetyltransferase (ChAT) buffer and for choline uptake in cultured human neuroblastoma (SK-N-SH) cells[3]
• for choline standard curve generation for quantifying phospholipase D (PLD) activity[4]
• as a component of slice solution for the dissection of entorhinal-hippocampal brain slices[5]

Sustratos

Sustrato de la colina acetiltransferasa

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 1
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable
• Equipo de protección personal: dust mask type N95 (US), Eyeshields, Gloves