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Key Documents

I2259

Sigma-Aldrich

myo-Inositol hexanicotinate

Synonym(s):

myo-Inositol hexa-3-pyridinecarboxylate, Inositol niacinate

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About This Item

Empirical Formula (Hill Notation):
C42H30N6O12
CAS Number:
Molecular Weight:
810.72
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:

mp

254-256 °C (lit.)

SMILES string

O=C(O[C@H]1[C@@H](OC(=O)c2cccnc2)[C@H](OC(=O)c3cccnc3)[C@@H](OC(=O)c4cccnc4)[C@H](OC(=O)c5cccnc5)[C@H]1OC(=O)c6cccnc6)c7cccnc7

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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[Use of derivative resolution for the spectrophotometric analysis of drug mixtures. I. Determination of inositol hexanicotinate and bamethan sulfate in tablets].
P Corti et al.
Bollettino chimico farmaceutico, 120(11), 657-667 (1981-11-01)
Huimin Qi et al.
International journal of biological macromolecules, 50(1), 270-272 (2011-11-26)
In this study, acetylated ulvan (AU) was prepared with acetic anhydride in N,N-dimethylacetamide, and the antihyperlipidemic activity of natural ulvan and its acetylated ulvan derivative (AU) in mice was determined. Obvious differences in antihyperlipidemic activity between natural ulvan and its
[Experience with the medical treatment of chronic cerebrovascular insufficiency: bamethan and inositol nicotinate versus placebo].
D Cucinotta et al.
Giornale di clinica medica, 62(5), 339-350 (1981-05-01)
L Harthon et al.
Arzneimittel-Forschung, 29(12), 1859-1862 (1979-01-01)
The esters between nicotinic acid and pentaerythritol (niceritrol, Perycit) or meso-inositol (MIHN) were hydrolyzed by enzymes present in plasma and tissues of man, rat and dog. Human plasma and rat tissues hydrolyzed niceritrol at a higher rate than did MIHN.
Yu Pengzhan et al.
Pharmacological research, 48(6), 543-549 (2003-10-07)
Ulvan, a sulfated polysaccharide from Ulva pertusa, was degraded to yield two low molecular weight fractions U1 and U2. The molecular weights of ulvan and its fractions were determined and varied from 151.6 to 28.2 kDa. They were fed to

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