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Merck

P6155

Sigma-Aldrich

Pyridoxal hydrochloride

BioReagent, suitable for cell culture, suitable for insect cell culture

Sinónimos:

3-Hydroxy-5-(hydroxymethyl)-2-methyl-4-pyridinecarboxaldehyde hydrochloride, PL HCl

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About This Item

Fórmula empírica (notación de Hill):
C8H9NO3 · HCl
Número de CAS:
Peso molecular:
203.62
Beilstein/REAXYS Number:
3656994
EC Number:
MDL number:
UNSPSC Code:
12352205
PubChem Substance ID:
NACRES:
NA.75

product line

BioReagent

Quality Level

assay

≥99% (HPLC)

form

powder

mol wt

Mw 203.62 g/mol

technique(s)

cell culture | insect: suitable
cell culture | mammalian: suitable

color

white to off-white

mp

173 °C (dec.) (lit.)

solubility

water: soluble 50 mg/mL, clear, colorless to light greenish-yellow

storage temp.

−20°C

SMILES string

Cl[H].[H]C(=O)c1c(CO)cnc(C)c1O

InChI

1S/C8H9NO3.ClH/c1-5-8(12)7(4-11)6(3-10)2-9-5;/h2,4,10,12H,3H2,1H3;1H

InChI key

FCHXJFJNDJXENQ-UHFFFAOYSA-N

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General description

Pyridoxal is a heterocyclic compound, weighing 167.2 Da. It is one of the natural forms of vitamin B6. Pyridoxal is found to be less stable than pyridoxine, hence heating might result in the loss of its action. Pyridoxal has a wide variety of sources and is present in both plants and animals. Pyridoxal serves as an efficient precursor for coenzymes : pyridoxal phosphate and pyridoxamine phosphate.

Application

Pyridoxal hydrochloride has been used to study its effect on cell proliferation and melanogenesis, using murine melanoma cells.
For the labeling of amino acids and their detection in picomolar amounts; Coenzymes and Cofactors, vol. 1: Vitamin B6, Pyridoxal Phosphate

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificados de análisis (COA)

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Nutritional Assessment (2016)
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Advanced nutrition: macronutrients, micronutrients, and metabolism (2015)
The effects of vitamin B6 compounds on cell proliferation and melanogenesis in B16F10 melanoma cells
Matsuo T, et al.
Oncology Letters, 15(4), 5181-5184 (2018)
Toshio Iwasaki et al.
Journal of the American Chemical Society, 131(38), 13659-13667 (2009-09-10)
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Nicotinamide adenine dinucleotide phosphate (NADP+) is essential for producing NADPH, the primary cofactor for reductive metabolism. We find that growth factor signaling through the phosphoinositide 3-kinase (PI3K)-Akt pathway induces acute synthesis of NADP+ and NADPH. Akt phosphorylates NAD kinase (NADK)

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