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Sevelamer HCl - 100%, high purity , CAS No.152751-57-0

    Grade & Purity:
  • 100%
In stock
Item Number
S413094
Grouped product items
SKU Size
Availability
Price Qty
S413094-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$260.90

FXR Inhibitors

Basic Description

Synonyms AB01568265_01 | FT-0653684 | 2-Propen-1-amine, hydrochloride (1:1), polymer with 2-(chloromethyl)oxirane | Sevelamer hydrochloride (JAN/USAN) | 2-(chloromethyl)oxirane;prop-2-en-1-amine;hydrochloride | HS-0082 | 2-Propen-1-amine Hydrochloride polymer with
Specifications & Purity 100%
Biochemical and Physiological Mechanisms Sevelamer HCl is a phosphate binding drug used to treat hyperphosphatemia via binding to dietary phosphate and prevents its absorption.
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Information

Sevelamer HCl Sevelamer HCl is a phosphate binding drug used to treat hyperphosphatemia via binding to dietary phosphate and prevents its absorption.


In vivo

Sevelamer is as effective as CaCO3 in reducing serum phosphorus, calcium-phosphorus product, and attenuating secondary hyperparathyroidism in nephrectomized rats (U) fed high phosphorus (HP) diet. Sevelamer results in markedly lower calcium deposition in the myocardium and aorta compared to control rats. Sevelamer suppresses calcification of the aorta media, and also the osteoid volume, fibrosis volume, and porosity ratio of femurs in chronic renal failure rats. Sevelamer results in a significantly lower degree of atherosclerosis and vascular calcification in uremic mice when compared with uremic control mice. Sevelamer exerts an effect on both intima and media calcification in uremic mice. Sevelamer treatment controlled serum P independent of increases in serum Ca, thus reducing serum calcium-phosphate product and further deterioration of renal function, as indicated by the highest creatinine clearances in uremic rats. Sevelamer is as effective as CaCO3 in the control of high-P-induced SH, as shown by similar serum PTH levels, parathyroid (PT) gland weight, and markers of PT hyperplasia. Sevelamer causes a dramatic reduction of renal Ca deposition compared with both uremic + high-P diet (U-HP) and the U-HP+CaCO3 diet. Sevelamer hydrochloride results in a fall in urine pH, as well as an increase in urinary ammonium and calcium excretion consistent with an increase in net acid excretion in animal model.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Epoxides
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Epoxides
Alternative Parents Oxacyclic compounds  Dialkyl ethers  Organopnictogen compounds  Organochlorides  Monoalkylamines  Hydrochlorides  Hydrocarbon derivatives  Alkyl chlorides  
Molecular Framework Not available
Substituents Dialkyl ether - Oxirane - Ether - Oxacycle - Alkyl chloride - Hydrocarbon derivative - Hydrochloride - Primary amine - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Primary aliphatic amine - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Alkyl halide - Aliphatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as epoxides. These are compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms).
External Descriptors Not available

Names and Identifiers

IUPAC Name 2-(chloromethyl)oxirane;prop-2-en-1-amine;hydrochloride
INCHI InChI=1S/C3H5ClO.C3H7N.ClH/c4-1-3-2-5-3;1-2-3-4;/h3H,1-2H2;2H,1,3-4H2;1H
InChIKey KHNXRSIBRKBJDI-UHFFFAOYSA-N
Smiles C=CCN.C1C(O1)CCl.Cl
Isomeric SMILES C=CCN.C1C(O1)CCl.Cl
PubChem CID 159247
Molecular Weight 186.08

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Solubility Solubility (25°C) In vitro 4-Methylpyridine 5 mg/mL warmed with 50ºC Water: bath DMSO: 0.005 mg/mL Water: Insoluble;
Molecular Weight 186.080 g/mol
XLogP3
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 2
Exact Mass 185.037 Da
Monoisotopic Mass 185.037 Da
Topological Polar Surface Area 38.600 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 55.100
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 1
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 3

Solution Calculators

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