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Sodium 1-octanesulfonate monohydrate

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

Synonym(s):

1-Octanesulfonic acid sodium salt monohydrate

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About This Item

Linear Formula:
CH3(CH2)6CH2SO3Na · H2O
CAS Number:
Molecular Weight:
234.29
Beilstein/REAXYS Number:
3574241
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:
NACRES:
NB.21

description

anionic

Quality Level

assay

≥99.0% (T)

form

sheet

quality

LiChropur

mol wt

234.29 g/mol

technique(s)

ion pair chromatography: 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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Low pressure ion pair chromatography with amperometric detection for the determination of trigonelline in coffee samples
Sousa MBT, et al.
Food Research International, 114, 223-229 (2018)
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

Reversed-phase HPLC sometimes requires ion pairing for adequate retention of polar compounds due to hydrophobic interactions.

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