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About This Item
Empirical Formula (Hill Notation):
C18H22N2O2
CAS Number:
Molecular Weight:
298.38
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
260-945-1
Beilstein/REAXYS Number:
3620576
MDL number:
grade
analytical standard
Quality Level
assay
≥98.5% (HPLC)
technique(s)
HPLC: suitable, gas chromatography (GC): suitable, solid phase extraction (SPE): suitable
mp
133-137 °C
application(s)
forensics and toxicology
pharmaceutical (small molecule)
veterinary
format
neat
storage temp.
2-8°C
SMILES string
CC(C)NCC(O)COc1cccc2[nH]c3ccccc3c12
InChI
1S/C18H22N2O2/c1-12(2)19-10-13(21)11-22-17-9-5-8-16-18(17)14-6-3-4-7-15(14)20-16/h3-9,12-13,19-21H,10-11H2,1-2H3
InChI key
BQXQGZPYHWWCEB-UHFFFAOYSA-N
General description
Standard for Supelco MIP SPE cartridges. For more information request Supelco Literature T407075, T706030, T706025
Application
Carazolol may be used as a reference standard for the determination of the analyte:
- In swine kidney by high-performance liquid chromatography with ultraviolet and fluorescence detection.
- In animal tissues by high-performance liquid chromatography with electrochemical detection.
Commission Regulation (EU) No 37/2010 of 22 December 2009 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Tomonaga Ozawa et al.
Bioorganic & medicinal chemistry, 19(17), 5231-5237 (2011-08-09)
We examined CH/π hydrogen bonds using an ab initio fragment molecular orbital (FMO) method, combined with the CHPI program, to evaluate complexes of active (bound with agonist 1) and inactive (bound with inverse agonist 2) β2 adrenergic receptor (β(2)AR) states.
Sid Topiol et al.
Biochemical pharmacology, 78(1), 11-20 (2009-05-19)
G-protein-coupled receptor (GPCR) proteins [Lundstrom KH, Chiu ML, editors. G protein-coupled receptors in drug discovery. CRC Press; 2006] are the single largest drug target, representing 25-50% of marketed drugs [Overington JP, Al-Lazikani B, Hopkins AL. How many drug targets are
Tony Warne et al.
Nature, 454(7203), 486-491 (2008-07-03)
G-protein-coupled receptors have a major role in transmembrane signalling in most eukaryotes and many are important drug targets. Here we report the 2.7 A resolution crystal structure of a beta(1)-adrenergic receptor in complex with the high-affinity antagonist cyanopindolol. The modified
Global Trade Item Number
| SKU | GTIN |
|---|---|
| T7383-25G | 04061837372759 |
| T3812-25G | 04061834409748 |
| 1649991-50MG | 04061838748430 |
| T3812-5G | 04061834409755 |
| T7383-100G | 04061833027479 |
| 1649991-100MG | 04065272400268 |
| PHR3140-100MG | 04065266116533 |
| 53787-10MG | 04061834391142 |
