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Merck

P9755

Pyridoxine hydrochloride

≥98% (HPLC)

Synonym(s):

Pyridoxine HCl, Adermine hydrochloride, PN HCl, Pyridoxol hydrochloride, Vitamin B6 hydrochloride

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About This Item

Empirical Formula (Hill Notation):
C8H11NO3 · HCl
CAS Number:
58-56-0
Molecular Weight:
205.64
NACRES:
NA.55
PubChem Substance ID:
24899059
eCl@ss:
34058008
UNSPSC Code:
12352205
EC Number:
200-386-2
MDL number:
MFCD00012807
Beilstein/REAXYS Number:
3632435

Key Documents

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SMILES string

Cl[H].Cc1ncc(CO)c(CO)c1O

InChI key

ZUFQODAHGAHPFQ-UHFFFAOYSA-N

InChI

1S/C8H11NO3.ClH/c1-5-8(12)7(4-11)6(3-10)2-9-5;/h2,10-12H,3-4H2,1H3;1H

assay

≥98% (HPLC)

form

powder

technique(s)

HPLC: suitable

color

white to off-white

mp

214-215 °C (lit.)

Quality Level

200

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Application

Pyridoxine hydrochloride has been used:
  • as a vitamin supplement in the basal medium for the cultivation of Bacillus mojavensis and Bacillus subtilis strains
  • as a supplement in pre-conditioning medium/MS salts to initiate somatic embryogenesis induction of Coffea canephora seeds
  • for oral administration in piglets to study its effect on the development of homocysteinemia

Biochem/physiol Actions

Pyridoxine/Vitamin B6 plays a key role in the nervous, immune, and endocrine systems. It is also involved in the metabolic processes of proteins, lipids, and carbohydrates. Deficiency of pyridoxine may lead to convulsions and epileptic encephalopathy and result in infant abnormalities.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H318

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

P9755-10G: + E009755-BULK: + P9755-RSAMPLE: + 2540118: + P9755-50G: + 2016230: + E009755-25G: + P9755-25G: + P9755-5G: + 2016230-20G: + P9755-5G-KC: + P9755-100G: + P9755-VAR: + E009755-100G: + P9755-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
SLCM1447
STBH9110
SLCL3820
STBK3570
SLCK2666

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Marie-Édith Côté-Robitaille et al.
Journal of nutritional science, 4, e31-e31 (2015-10-27)
Homocysteine (Hcy) is an intermediary sulphur amino acid recognised for pro-oxidative properties in several species which may weaken immune competence in piglets. In this species, there is an acute 10-fold increase of concentrations of plasma Hcy (pHcy) during the first
Liat Ashkenazi-Hoffnung et al.
The Israel Medical Association journal : IMAJ, 15(1), 23-26 (2013-03-15)
Diclectin (pyridoxine 10 mg and doxylamine 10 mg) has traditionally been used to treat nausea and vomiting of pregnancy (NVP); however, this drug is unavailable in many countries. To evaluate the efficacy and safety of a simple bi-daily treatment regimen
Manfred Eggersdorfer et al.
Angewandte Chemie (International ed. in English), 51(52), 12960-12990 (2012-12-05)
The discovery of vitamins as essential factors in the diet was a scientific breakthrough that changed the world. Diseases such as scurvy, rickets, beriberi, and pellagra were recognized to be curable with an adequate diet. These diseases had been prevalent
Sonia Fargue et al.
Biochimica et biophysica acta, 1832(10), 1776-1783 (2013-04-20)
Primary hyperoxaluria type 1 (PH1) is a rare hereditary calcium oxalate kidney stone disease caused by a deficiency of the liver-specific pyridoxal-phosphate-dependent peroxisomal enzyme alanine:glyoxylate aminotransferase (AGT). About one third of patients are responsive to pharmacological doses of pyridoxine (vitamin
Riccardo Montioli et al.
Human molecular genetics, 22(8), 1615-1624 (2013-01-17)
Dopa or aromatic amino acid decarboxylase (DDC, AADC) is a pyridoxal 5'-phosphate-dependent enzyme that catalyses the production of the neurotransmitters dopamine and serotonin. Among the so far identified mutations associated with AADC deficiency, an inherited rare neurometabolic disease, the S250F
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