carazolol structure
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Common Name | carazolol | ||
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CAS Number | 57775-29-8 | Molecular Weight | 298.38 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 531.2±40.0 °C at 760 mmHg | |
Molecular Formula | C18H22N2O2 | Melting Point | 133-137 °C | |
MSDS | Chinese USA | Flash Point | 275.1±27.3 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of carazololCarazolol is a β1/β2 adrenoceptor antagonist of high potency used in the research of hypertension. Carazolol is also a potent, selective β3-adrenoceptor agonist[1]. |
Name | carazolol hcl |
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Synonym | More Synonyms |
Description | Carazolol is a β1/β2 adrenoceptor antagonist of high potency used in the research of hypertension. Carazolol is also a potent, selective β3-adrenoceptor agonist[1]. |
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Related Catalog | |
Target |
β1 adrenoceptor β2 adrenoceptor β3 adrenoceptor |
In Vivo | Carazolol (0.01 mg/kg; i.m.; once) shows no significant side effects[2]. Animal Model: Kivircik sheeps, 25-45 kg, nonpregnant[2] Dosage: 0.01 mg/kg Administration: Intramuscular injection, once Result: Urea, creatinin, ALT, ALP, GGT, LDH, Ca, P, T.Protein, Mg, Cu levels in blood serum parameters were found to be in normal level however serum Fe, Zn levels were decreased. |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 531.2±40.0 °C at 760 mmHg |
Melting Point | 133-137 °C |
Molecular Formula | C18H22N2O2 |
Molecular Weight | 298.38 |
Flash Point | 275.1±27.3 °C |
Exact Mass | 298.168121 |
PSA | 57.28000 |
LogP | 3.59 |
Vapour Pressure | 0.0±1.5 mmHg at 25°C |
Index of Refraction | 1.652 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
Hazard Codes | Xn: Harmful; |
Risk Phrases | R22 |
Safety Phrases | S26 |
RIDADR | NONH for all modes of transport |
RTECS | UA8685000 |
HS Code | 2933990090 |
Precursor 0 | |
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DownStream 2 | |
HS Code | 2933990090 |
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Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Determination of 15 sedative residues in mutton by rapid resolution liquid chromatography-tandem mass spectrometry.
J. Sci. Food Agric. 95(3) , 598-606, (2015) The use of xenobiotic compounds in animal husbandry has given rise to consumer anxieties regarding residual risk and food safety. Thus, animal tissues have become main samples for residue analysis and... |
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Lipophilicity of basic drugs measured by hydrophilic interaction chromatography.
J. Med. Chem. 52 , 3416-9, (2009) RPLC gains acceptance in pharmaceutical research for the rapid determination of lipophilicity but remains limited for the determination of partition coefficients of moderate to strong basic compounds ... |
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Constitutive phospholipid scramblase activity of a G protein-coupled receptor.
Nat. Commun. 5 , 5115, (2014) Opsin, the rhodopsin apoprotein, was recently shown to be an ATP-independent flippase (or scramblase) that equilibrates phospholipids across photoreceptor disc membranes in mammalian retina, a process... |
Conduction |
1-(9H-Carbazol-4-yloxy)-3-[(1-methylethyl)amino]-2-propanol |
1-(9H-carbazol-4-yloxy)-3-(propan-2-ylamino)propan-2-ol |
carazolol |
CARAZOLOL HYDROCHLORIDE |
1-(9H-Carbazol-4-yloxy)-3-(isopropylamino)-2-propanol |
EINECS 260-945-1 |
1-(9H-Carbazol-4-yloxy)-3-(isopropylamino)propan-2-ol |
suacron |
MFCD03428052 |
2-Propanol, 1-(9H-carbazol-4-yloxy)-3-[(1-methylethyl)amino]- |
Carazololum |
Conducton |