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481907

Nicotinamide

Precursor of the coenzymes NAD+ and NADP+.

Synonym(s):

Nicotinamide, Niacinamide, Nicotinic Acid Amide

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About This Item

Empirical Formula (Hill Notation):
C6H6N2O
CAS Number:
98-92-0
Molecular Weight:
122.12
MDL number:
MFCD00006395
UNSPSC Code:
41116107
NACRES:
NA.25

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Quality Level

200

assay

≥99% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
protect from light

impurities

≤0.2% Nicotinic acid (TLC)

color

white

solubility

water: soluble

cation traces

heavy metals (as Pb): ≤0.003%

shipped in

ambient

storage temp.

15-25°C

SMILES string

NC(=O)c1cnccc1

InChI

1S/C6H6N2O/c7-6(9)5-2-1-3-8-4-5/h1-4H,(H2,7,9)

InChI key

DFPAKSUCGFBDDF-UHFFFAOYSA-N

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This Item
7234072345N0600000
Nicotinamide Precursor of the coenzymes NAD+ and NADP+.

Millipore

481907

Nicotinamide

Nicotinamide ≥99.5% (HPLC)

Sigma-Aldrich

72340

Nicotinamide

Nicotinamide ≥98.5% (HPLC)

Sigma-Aldrich

72345

Nicotinamide

Nicotinamide European Pharmacopoeia (EP) Reference Standard

N0600000

Nicotinamide

assay

≥99% (HPLC)

assay

≥99.5% (HPLC)

assay

≥98.5% (HPLC)

assay

-

form

solid

form

powder or crystals

form

powder

form

solid

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

-

manufacturer/tradename

Calbiochem®

manufacturer/tradename

-

manufacturer/tradename

-

manufacturer/tradename

EDQM

storage temp.

15-25°C

storage temp.

-

storage temp.

-

storage temp.

2-8°C

storage condition

OK to freeze, protect from light

storage condition

-

storage condition

-

storage condition

-

General description

Precursor of the coenzymes NAD+ and NADP+.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Irritant (B)

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

302.0 °F - closed cup

flash_point_c

150 °C - closed cup

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Xing Jian et al.
Nature communications, 12(1), 4338-4338 (2021-07-17)
Previous GWAS studies identified non-coding loci with parent-of-origin-specific effects on Type 2 diabetes susceptibility. Here we report the molecular basis for one such locus near the KRTAP5-6 gene on chromosome 11. We determine the pattern of long-range contacts between an enhancer
Laszlo A Groh et al.
Immunometabolism, 3(3), e210025-e210025 (2021-07-17)
Following brief exposure to endogenous atherogenic particles, such as oxidized low-density lipoprotein (oxLDL), monocytes/macrophages can adopt a long-term pro-inflammatory phenotype, which is called trained immunity. This mechanism might contribute to the chronic low-grade inflammation that characterizes atherosclerosis. In this study
Ok-Seon Kwon et al.
Cancers, 12(4) (2020-04-12)
The role of Situin 1 (SIRT1) in tumorigenesis is still controversial due to its wide range of substrates, including both oncoproteins and tumor suppressors. A recent study has demonstrated that SIRT1 interferes in the Kirsten rat sarcoma viral oncogene homolog
Ming Hu et al.
Cell reports, 34(5), 108703-108703 (2021-02-04)
Using chromatin conformation capture, we show that an enhancer cluster in the STARD10 type 2 diabetes (T2D) locus forms a defined 3-dimensional (3D) chromatin domain. A 4.1-kb region within this locus, carrying 5 T2D-associated variants, physically interacts with CTCF-binding regions
Ildem Akerman et al.
Cell reports, 35(2), 108981-108981 (2021-04-15)
Despite the central role of chromosomal context in gene transcription, human noncoding DNA variants are generally studied outside of their genomic location. This limits our understanding of disease-causing regulatory variants. INS promoter mutations cause recessive neonatal diabetes. We show that

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