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Merck

53787

Carazolol

analytical standard

Sinonimo/i:

1-(Carbazol-4-yloxy)-3-(isopropylamino)-2-propanol, 4-(2-Hydroxy-3-isopropylamino-propoxy)carbazole

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10 MG

161,25 €

161,25 €

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Informazioni su questo articolo

Formula empirica (notazione di Hill):
C18H22N2O2
Numero CAS:
57775-29-8
Peso molecolare:
298.38
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757996
EC Number:
260-945-1
Beilstein/REAXYS Number:
3620576
MDL number:
MFCD00864588

Documenti fondamentali

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Nome del prodotto

Carazolol, analytical standard

InChI key

BQXQGZPYHWWCEB-UHFFFAOYSA-N

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

SMILES string

CC(C)NCC(O)COc1cccc2[nH]c3ccccc3c12

grade

analytical standard

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

Quality Level

200

Categorie correlate

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Carazolol analytical standard

Supelco

53787

Carazolol

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49358

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Tulobuterol VETRANAL®, analytical standard

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53541

Tulobuterol

Salbutamol VETRANAL®, analytical standard

Supelco

46725

Salbutamol

technique(s)

HPLC: suitable, solid phase extraction (SPE): suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable, solid phase extraction (SPE): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable, solid phase extraction (SPE): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

application(s)

clinical testing

format

neat

format

neat

format

neat

format

neat

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

100

grade

analytical standard

grade

analytical standard

grade

analytical standard

grade

analytical standard

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

-

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.[1]
  • In animal tissues by high-performance liquid chromatography with electrochemical detection.[2]

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.

General description

Standard for Supelco MIP SPE cartridges. For more information request Supelco Literature T407075, T706030, T706025

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Related product

N° Catalogo
Descrizione
Determinazione del prezzo

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Classe di stoccaggio

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

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
0000401292
0000401292
WXBF3309V
0000280507
WXBF1115V

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Determination of tranquilisers and carazolol residues in animal tissue using high-performance liquid chromatography with electrochemical detection.
Rose MD and Shearer G
Journal of Chromatography A, 624(1-2), 471- 477 (1992)
Karin A Stephenson et al.
Journal of medicinal chemistry, 51(16), 5093-5100 (2008-07-29)
An efficient and general method has been developed for fluorine-18 labeling of beta-blockers that possess the propanolamine moiety. A new synthetically versatile intermediate, 3-(1-(benzyloxy)propan-2-yl)-2-oxooxazolidin-5-yl)methyl 4-methylbenzenesulfonate (13), was prepared and can be conjugated to any phenoxy core. To demonstrate the synthetic
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
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