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Supelco

Sodium 1-octanesulfonate monohydrate

suitable for ion pair chromatography, LiChropur, ≥99.0% (T)

Synonym(s):
1-Octanesulfonic acid sodium salt monohydrate
Linear Formula:
CH3(CH2)6CH2SO3Na · H2O
CAS Number:
Molecular Weight:
234.29
Beilstein:
3574241
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NB.21

Quality Level

description

anionic

assay

≥99.0% (T)

quality

LiChropur

mol wt

234.29 g/mol

technique(s)

HPLC: suitable
ion pair chromatography: suitable
protein purification: suitable

mp

≥300 °C (lit.)

λ

10 % in H2O

UV absorption

λ: 210 nm Amax: 0.1
λ: 220 nm Amax: 0.06
λ: 230 nm Amax: 0.04
λ: 260 nm Amax: 0.02
λ: 500 nm Amax: 0.02

suitability

corresponds to standard for RP gradient test
corresponds to standard for filter test

SMILES string

O.[Na+].CCCCCCCCS([O-])(=O)=O

InChI

1S/C8H18O3S.Na.H2O/c1-2-3-4-5-6-7-8-12(9,10)11;;/h2-8H2,1H3,(H,9,10,11);;1H2/q;+1;/p-1

InChI key

MBURIAHQXJQKRE-UHFFFAOYSA-M

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General description

Sodium 1-octanesulfonate monohydrate is an ion-pair reagent suitable for cation separation sorted by carbon chain length.

Application

Sodium 1-octanesulfonate monohydrate may be used as an ion pair reagent for the determination of trigonelline in coffee samples by ion-pair chromatography. It may also be used as a mobile phase additive and diluent in the identification, assay and impurity profile analysis of methylseleno-L-cysteine (L-SeMC) bulk drug by reversed-phase ion-pairing HPLC method with UV detection.

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Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificate of Analysis

Certificate of Origin

More documents

Quotes and Ordering

Rapid and simple analysis of paraquat in tissue homogenate by ultra-high performance liquid chromatography.
Merritt, T. J. S., et al.
Analytical Methods : Advancing Methods and Applications, 3, 1428-1432 (2011)
Validation of a Stability-Indicating Method for Methylseleno-l-Cysteine (l-SeMC)
Canady K, et al.
Journal of Chromatographic Science, 54(1), 22-27 (2016)
Kamila Syslová et al.
Journal of chromatography. A, 1218(21), 3382-3391 (2011-03-15)
A sensitive assay method was developed for a parallel, rapid and precise determination of dopamine and its metabolites, homovanillic acid, 3-methoxytyramine and 3,4-dihydroxyphenylacetic acid, from brain microdialysates. The method consisted of a pre-treatment step, freeze-drying (lyophilization), to concentrate dopamine and
Maria Addolorata Saracino et al.
Journal of pharmaceutical and biomedical analysis, 104, 122-129 (2014-12-17)
A new microextraction by packed sorbent (MEPS) procedure coupled to a high-performance liquid chromatographic method has been developed for quantitation of catecholamines (i.e. norepinephrine, epinephrine and dopamine) in innovative biological samples, namely dried plasma and urine spots. Analyses were carried

Protocols

Analysis of Difficult Polar Compounds using Sigma-Aldrich Ion Pair Reagents and Supelco Ascentis HPLC Columns

Because reversed-phase HPLC is primarily dependent on hydrophobic interactions between the stationary phase and analyte, ion pairing is occasionally necessary to obtain sufficient retention of polar, ionizable compounds.

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