Advanced Search



Amiloride hydrochloride hydrate

SIGMA/A7410 - ≥98% (HPLC), powder

Synonym: N-Amidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride hydrate

CAS Number: 2016-88-8 (anhydrous)
Empirical Formula (Hill Notation): C6H8ClN7O · HCl · xH2O
Molecular Weight: 266.09 (anhydrous basis)
MDL Number: MFCD03703482
Linear Formula: C6H8ClN7O · HCl · xH2O
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-A7410-1G 1 g
$83.90
1/EA
Add To Favorites
45-A7410-5G 5 g
$351.00
1/EA
Add To Favorites
45-A7410-10G 10 g
$500.00
1/EA
Add To Favorites

 

assay ≥98% (HPLC)
color , White to Yellow and Faint Green to Green and Yellow-Green
form powder
InChI 1S/C6H8ClN7O.ClH.H2O/c7-2-4(9)13-3(8)1(12-2)5(15)14-6(10)11;;/h(H4,8,9,13)(H4,10,11,14,15);1H;1H2
InChI key WDZJJRLYFQNCQL-UHFFFAOYSA-N
mp 285-288 °C (dec.)
originator Perrigo
Quality Level 200 
SMILES string O.Cl.NC(=N)NC(=O)c1nc(Cl)c(N)nc1N
solubility H2O: 50 mg/mL, hazy (Very Faint Yellow to Dark Yellow and Very Faint Green-Yellow to Dark Green-Yellow and Very Faint Brown-Yellow to Dark Brown-Yellow)
storage temp. room temp
Application: Amiloride is a selective T-type calcium channel blocker, an epithelial sodium channel blocker and a selective inhibitor of urokinase plasminogen activator (uPA). Amiloride has been used in a study to develop an alternative treatment for constipation.
Biochem/physiol Actions: Selective T-type Ca2+ and epithelial sodium channel blocker
Biochem/physiol Actions: Selective T-type calcium channel blocker and blocker of epithelial sodium channel. Selective inhibitor of urokinase plasminogen activator (uPA).
Disclaimer: Protect from light.
Features and Benefits: This compound is a featured product for ADME Tox research. Click here  to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm .
Features and Benefits: This compound is featured on the Acid-Sensing (Proton-gated) Ion Channels (ASICs)  and Imidazoline Binding Sites  pages of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here .
Features and Benefits: This compound was developed by Perrigo . To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here .
Symbol GHS06  GHS06
Signal word Danger
Hazard statements H301
Precautionary statements P301 + P330 + P331 + P310
Hazard Codes T
Risk Statements 25
Safety Statements 45
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
mp 285-288 °C (dec.)
Storage Temp. room temp
UNSPSC 12352200

The following items have been added to your cart:

Choose a favorite list for this item:

Catalog Number Description Price
$

Returns/Order support

Please fill out the form below if you want to request order support from Krackeler Scientific.


Quick Order

* Required


New Year Price Updates

We are currently working diligently to update our website pricing information for the New Year. If you place an order, you will be acknowledged with any corrected pricing. If you'd like the most current information sooner, please don't hesitate to drop us an email or give us a call and we'd be happy to assist. Thank you for your patience while we are updating.

800-334-7725
office@krackeler.com


Play Video

To Request a Quote

  1. Search or Browse for items and add to them to your Shopping Cart.
  2. Click the "Request Quote" button at the bottom of the Shopping Cart page.
  3. Fill out required fields.
  4. Optionally you can convert to standard checkout mode by choosing a payment type.
  5. Click "Request Quote" at the bottom of the page.

You will be contacted with a quote.

To Order From a Quote

  1. Register and login to the website.
  2. Receive a quote from your sales representative or customer service.
  3. Have your copy of the quote in hand.
  4. Visit our quote module to search for your quote.
Back to Top