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C2632

Sigma-Aldrich

CAPS

≥99%

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:
NACRES:
NA.25
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Quality Level

Assay

≥99%

form

crystalline powder

pH

3.0-7.0

pKa (25 °C)

10.4

pKa 

10.4

mp

>300 °C (lit.)

solubility

H2O: soluble 15g + 85 mL, clear, colorless

application(s)

diagnostic assay manufacturing

SMILES string

OS(=O)(=O)CCCNC1CCCCC1

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239782C6070RDD015
CAPS ≥99%

C2632

CAPS

CAPS ULTROL® Grade, ≥99% (HPLC), zwitterionic buffer useful in pH range 7.9-11.1

239782

CAPS

CAPS BioXtra, ≥99%

C6070

CAPS

CAPS anhydrous, free-flowing, Redi-Dri™, ≥99%

RDD015

CAPS

assay

≥99%

assay

≥99% (HPLC)

assay

≥99%

assay

≥99%

Quality Level

400

Quality Level

200

Quality Level

400

Quality Level

100

application(s)

diagnostic assay manufacturing

application(s)

-

application(s)

-

application(s)

-

form

crystalline powder

form

solid

form

powder

form

powder

solubility

H2O: soluble 15g + 85 mL, clear, colorless

solubility

water: 20 mg/mL

solubility

H2O: 0.5 M at 20 °C, clear, colorless

solubility

water: 15 % (w/w), clear, colorless

pH

3.0-7.0

pH

-

pH

3.0-7.0 (20 °C, 0.5 M in H2O)

pH

3.0-7.0

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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S C Perricone et al.
Journal of medicinal chemistry, 37(22), 3693-3700 (1994-10-28)
Random screening identified N,N'-dicyclohexyl-4-morpholinecarboxamidine (U-18177, 1) as an orally effective nonkaliuretic diuretic in rats. The diuretic profile of 1 and its 1-adamantyl analog (U-37883A, 4) was confirmed orally in dogs, when they were less potent than standard diuretics but showed
Earl R Kern et al.
Antimicrobial agents and chemotherapy, 46(4), 991-995 (2002-03-19)
The nucleotide phosphonates cidofovir (CDV) and cyclic cidofovir (cCDV) are potent antiviral compounds when administered parenterally but are not well absorbed orally. These compounds have been reported to have activity against orthopoxvirus replication in vitro and in animal models when
Yuji Kamata et al.
Hypertension research : official journal of the Japanese Society of Hypertension, 32(3), 220-226 (2009-03-06)
It is suggested that an ATP-sensitive potassium channel blocker suppresses sodium-induced hypertension through increased secretion of urinary kallikrein. We reported that glibenclamide, an ATP-sensitive potassium channel blocker, accelerated dose-dependent secretion of renal kallikrein in sliced kidney cortex and in vivo

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