51835
Sodium 1-heptanesulfonate monohydrate
≥96.0% (T)
Synonym(s):
1-Heptanesulfonic acid sodium salt monohydrate
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
CH3(CH2)5CH2SO3Na · H2O
CAS Number:
Molecular Weight:
220.26
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
245-210-5
Beilstein/REAXYS Number:
3731762
MDL number:
Assay:
≥96.0% (T)
Form:
solid
Quality Level
assay
≥96.0% (T)
form
solid
functional group
sulfonic acid
SMILES string
O.[Na+].CCCCCCCS([O-])(=O)=O
InChI
1S/C7H16O3S.Na.H2O/c1-2-3-4-5-6-7-11(8,9)10;;/h2-7H2,1H3,(H,8,9,10);;1H2/q;+1;/p-1
InChI key
XWZCREJRXRKIRQ-UHFFFAOYSA-M
Application
Sodium 1-heptanesulfonate monohydrate can be used as:
- A catalyst to synthesize 2-aryl-1-arylmethyl-1H-benzo[d]imidazoles through the condensation reaction of o-phenylenediamine with various aromatic aldehydes.
- An ion-pair reagent for HPLC-UV analysis.
Disclaimer
may discolor on storage
Still not finding the right product?
Explore all of our products under Sodium 1-heptanesulfonate monohydrate
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Development and Validation of an HPLC Assay For Dual Detection of Gentamicin Sulfate and Leucine From a Novel Dry Powder For Inhalation.
Kuehl PJ, et al.
Journal of Analytical and Bioanalytical Techniques , 3(152), 2-2 (2012)
Visible-Light-Driven Photoreactions of [(bpy)2Ru (II) L]Cl2 in Aqueous Solutions (bpy= Bipyridine, L= 1,2-Bis (4-(4'-methyl)-2, 2'-bipyridyl) Ethene).
Zhang H, et al.
The Journal of Physical Chemistry A, 112(5), 808-817 (2008)
Martin Kögler et al.
Journal of medicinal chemistry, 54(13), 4847-4862 (2011-06-11)
A series of 5-substituted 2'-deoxyuridine monophosphate analogues has been synthesized and evaluated as potential inhibitors of mycobacterial ThyX, a novel flavin-dependent thymidylate synthase in Mycobacterium tuberculosis. A systematic SAR study led to the identification of compound 5a, displaying an IC(50)