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H2766

Sigma-Aldrich

Sodium 1-heptanesulfonate

Synonym(s):

1-Heptanesulfonic acid sodium salt

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About This Item

Linear Formula:
C7H15O3SNa
CAS Number:
Molecular Weight:
202.25
EC Number:
MDL number:
UNSPSC Code:
12161900
PubChem Substance ID:
NACRES:
NA.21

biological source

synthetic (oragnic)

Quality Level

description

anionic

form

powder

mol wt

202.25 g/mol

technique(s)

HPLC: suitable
LC/MS: suitable

impurities

<2.0% water (Karl Fischer)

mp

300  °C (572 °F)

solubility

H2O: ≥100 mg/mL

cation traces

Na: 10.8-12.0 % (w/v) (anhydrous)

SMILES string

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

InChI

1S/C7H16O3S.Na/c1-2-3-4-5-6-7-11(8,9)10;/h2-7H2,1H3,(H,8,9,10);/q;+1/p-1

InChI key

REFMEZARFCPESH-UHFFFAOYSA-M

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General description

Sodium 1-heptanesulfonate belongs to the sodium alkylsulfonate group of surfactants. It has a -SO?3 head group with sodium and an alkyl chain attached to the head group. Sodium 1-heptanesulfonate has a critical micelle concentration value of 0.302 mol/dm3.
Sodium 1-heptanesulfonate, also known as sodium heptanesulfonate, is a versatile compound commonly used in lab experiments and biochemical research. It acts as an ion-pairing agent, surfactant, and buffer, playing a crucial role in various applications. In biochemistry, it helps with tasks like protein purification and nucleic acid separation by reducing surface tension for better mixing. It also serves as a chelating agent for metal ion analysis and acts as a buffer in biological experiments. Sodium 1-heptanesulfonate is a preferred choice in HPLC and high-performance capillary electrophoresis analyses, aiding in the separation of positively charged analytes in both organic and inorganic compounds, from pharmaceuticals to peptide research.

Application

Sodium 1-heptanesulfonate has been used as a component of the mobile phase buffer for preequilibration of high performance liquid chromatography column.
Ion-pairing reagent for HPLC, including analyses of peptides and proteins.

Biochem/physiol Actions

Sodium 1-heptanesulfonate serves as an ion-pairing reagent for analysis of epinephrine and norepinephrine in ion-pairing chromatography (IPC).

Features and Benefits

  • Ideal for Cell Biology and Biochemical Research
  • High purity chemical suitable for multiple research applications

Other Notes

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comparable product

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Analysis of catecholamines in urine by unique LC/MS suitable ion-pairing chromatography
Bergmann ML, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 1057(2), 118-123 (2017)
Determination of S-adenosylmethionine and S-adenosylhomocysteine from human blood samples by HPLC-FL
Birsan C, et al.
Analytical Letters, 41(10), 1720-1731 (2008)
Validated HPLC-Fl method for the analysis of S-adenosylmethionine and S-adenosylhomocysteine biomarkers in human blood
Albu C, et al.
Journal of Fluorescence, 23(3), 381-386 (2013)
A R Calhoun et al.
Journal of colloid and interface science, 309(2), 505-510 (2007-03-03)
Measurements have been made to determine the solubility of ethane, C2H6, in aqueous solutions of four different surfactants of the linear alkanesulfonate class at 25 degrees C. The surfactants, sodium 1-pentanesulfonate, sodium 1-hexanesulfonate, sodium 1-heptanesulfonate, and sodium 1-octanesulfonate, all share
Takeshi Oshizaka et al.
International journal of pharmaceutics, 475(1-2), 292-297 (2014-08-27)
Skin concentrations of topically administered compounds need to be considered in order to evaluate their efficacies and toxicities. This study investigated the relationship between the skin permeation and concentrations of compounds, and also predicted the skin concentrations of these compounds

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