V900307
CAPS
Vetec™, reagent grade, ≥98%
Synonym(s):
3-(Cyclohexylamino)-1-propanesulfonic acid
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About This Item
Linear Formula:
C6H11NH(CH2)3SO3H
CAS Number:
Molecular Weight:
221.32
Beilstein:
2835588
EC Number:
MDL number:
UNSPSC Code:
12161700
PubChem Substance ID:
grade
reagent grade
product line
Vetec™
Assay
≥98%
form
powder
pH
3.0-7.0
pKa
10.4
mp
>300 °C (lit.)
solubility
water: 0.176 g/mL, clear, colorless
SMILES string
OS(=O)(=O)CCCNC1CCCCC1
InChI
1S/C9H19NO3S/c11-14(12,13)8-4-7-10-9-5-2-1-3-6-9/h9-10H,1-8H2,(H,11,12,13)
InChI key
PJWWRFATQTVXHA-UHFFFAOYSA-N
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Leo Lebanov et al.
The Analyst, 145(17), 5897-5904 (2020-07-17)
This work provides the pKa at the biorelevant temperature of 37 °C for a set of compounds proposed as internal standards for the internal standard capillary electrophoresis (IS-CE) method. This is a high throughput method that allows the determination of
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Frances E Lock et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(34), E3534-E3543 (2014-08-13)
Remnants of ancient transposable elements (TEs) are abundant in mammalian genomes. These sequences harbor multiple regulatory motifs and hence are capable of influencing expression of host genes. In response to environmental changes, TEs are known to be released from epigenetic
L Mikael Broman et al.
Critical care (London, England), 19, 278-278 (2015-07-15)
In severe respiratory and/or circulatory failure, extracorporeal membrane oxygenation (ECMO) may be a lifesaving procedure. Specialized departments provide ECMO, and these patients often have to be transferred for treatment. Conventional transportation is hazardous, and deaths have been described. Only a
Yi-Hsun Chang et al.
The Journal of biological chemistry, 282(47), 34306-34314 (2007-09-26)
3alpha-hydroxysteroid dehydrogenase/carbonyl reductase from Comamonas testosteroni catalyzes the oxidation of androsterone with NAD(+) to form androstanedione and NADH with a concomitant releasing of protons to bulk solvent. To probe the proton transfer during the enzyme reaction, we used mutagenesis, chemical
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