N-Acetyltyramine
Suppliers
Names
[ CAS No. ]:
1202-66-0
[ Name ]:
N-Acetyltyramine
[Synonym ]:
GNF-PF-5230
N-Acetyltyramine
N-acetyltyramin
N-[2-(4-Hydroxyphenyl)ethyl]acetamide
Acetamide, N-[2-(4-hydroxyphenyl)ethyl]-
Chemical & Physical Properties
[ Density]:
1.1±0.1 g/cm3
[ Boiling Point ]:
424.1±28.0 °C at 760 mmHg
[ Melting Point ]:
134°C
[ Molecular Formula ]:
C10H13NO2
[ Molecular Weight ]:
179.216
[ Flash Point ]:
210.3±24.0 °C
[ Exact Mass ]:
179.094635
[ PSA ]:
49.33000
[ LogP ]:
0.39
[ Vapour Pressure ]:
0.0±1.0 mmHg at 25°C
[ Index of Refraction ]:
1.546
[ Storage condition ]:
2-8°C
MSDS
Toxicological Information
CHEMICAL IDENTIFICATION
- RTECS NUMBER :
- AC3852300
- CHEMICAL NAME :
- Acetamide, N-(2-(4-hydroxyphenyl)ethyl)-
- CAS REGISTRY NUMBER :
- 1202-66-0
- BEILSTEIN REFERENCE NO. :
- 2096467
- LAST UPDATED :
- 199612
- DATA ITEMS CITED :
- 1
- MOLECULAR FORMULA :
- C10-H13-N-O2
- MOLECULAR WEIGHT :
- 179.24
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intravenous
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- >500 mg/kg
- TOXIC EFFECTS :
- Behavioral - changes in motor activity (specific assay) Cardiac - cardiomyopathy including infarction Skin and Appendages - hair
- REFERENCE :
- APTOA6 Acta Pharmacologica et Toxicologica. (Copenhagen, Denmark) V.1-59, 1945-86. For publisher information, see PHTOEH Volume(issue)/page/year: 38,474,1976
Safety Information
[ Symbol ]:
GHS05
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H318
[ Precautionary Statements ]:
P280-P305 + P351 + P338
[ Hazard Codes ]:
Xi
[ RIDADR ]:
NONH for all modes of transport
[ HS Code ]:
2924299090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2924299090
[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Articles
Anal. Chem. 81(10) , 4089-98, (2009)
N-acetyltyramine was synthesized and electropolymerized together with a negatively charged sulfobutylether-beta-cyclodextrin on a boron-doped diamond (BDD) electrode followed by the electropolymerizat...
Biochemistry 53(49) , 7777-93, (2014)
Arylalkylamine N-acetyltransferase (AANAT) catalyzes the penultimate step in the biosynthesis of melatonin and other N-acetylarylalkylamides from the corresponding arylalkylamine and acetyl-CoA. The N...
Acta Pharmacol. Toxicol. (Copenh.) 40(2) , 247-58, (1977)
The effect of five sympathomimetic amines and some of their acetyl derivatives on the blood pressure of the rat was determined on the left carotid artery. After pretreatment with chlorisondamine (1 mg...