Chloroquine diphosphate salt

Product Name: Chloroquine diphosphate salt

Synonym: N⁴-(7-Chloro-4-quinolinyl)–N¹,N¹–dimethyl-1,4-pentanediamine diphosphate salt

CAS Number: 50-63-5
Empirical Formula (Hill Notation): C₁₈H₂₆ClN₃ · 2H₃PO₄
Molecular Weight: 515.86
Beilstein Registry Number: 4223142
EC Number: 200-055-2
MDL Number: MFCD00069852
Linear Formula: C₁₈H₂₆ClN₃ · 2H₃PO₄
Product Type: Chemical

CAS NO: 97792-45-5Angiotensin-converting Enzyme (ACE) inhibitors
Assay: ≥98%
Form: solid
impurities
≤2% water
InChI Key
QKICWELGRMTQCR-UHFFFAOYSA-N
Mode of action
enzyme | inhibits
mp
200 °C (dec.)(lit.)
Application: DNA intercalator. Also used to increase transfection efficiency.
Biochem/physiol Actions:
Standard anti-malarial drug. Substrate for MRP in multidrug resistant cell line and inhibits photoaffinity labeling of MRP by quinoline-based photoactive drug IAAQ (N-[4-[1-hydroxy-2-(dibutylamino)ethyl]quinolin-8-yl]-4-azidosalicylamide).
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 also offered as part of Sigma′s Library of Pharmacologically Active Compounds (LOPAC®1280), a biologically annotated collection of high-quality, ready-to-screen compounds. Click here to learn more.
Legal InFormation: LOPAC is a registered trademark of Sigma-Aldrich Co. LLC
Packaging:
25, 50, 100, 250 g in glass bottle
Symbol
GHS07
Signal word
Warning
Hazard statements
H302
Hazard Codes
Xn
Risk Statements
22
Safety Statements
22-24/25
RIDADR: NONH for all modes of transport
WGK Germany: 3
RTECS
VB2450000
Purity: ≥98%
mp
200 °C (dec.)(lit.)
UNSPSC
12352107
PubMed ID:http://jpet.aspetjournals.org/content/89/1/64