H1754
DL-β-Hydroxyphenethylamine
Synonym(s):
2-Amino-1-phenylethanol, α-(Aminomethyl)benzyl alcohol, DL-β-Hydroxyphenethylamine, Phenylethanolamine
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About This Item
Linear Formula:
NH2CH2CH(OH)C6H5
CAS Number:
Molecular Weight:
137.18
EC Number:
231-469-1
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
971222
MDL number:
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
160 °C/17 mmHg (lit.)
mp
56-58 °C (lit.)
format
neat
SMILES string
NCC(O)c1ccccc1
InChI
1S/C8H11NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8,10H,6,9H2
InChI key
ULSIYEODSMZIPX-UHFFFAOYSA-N
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Qian Wu et al.
Journal of medicinal chemistry, 48(23), 7243-7252 (2005-11-11)
The X-ray structure of human phenylethanolamine N-methyltransferase (hPNMT) complexed with its product, S-adenosyl-L-homocysteine (4), and the most potent inhibitor reported to date, SK&F 64139 (7), was used to identify the residues involved in inhibitor binding. Four of these residues, Val53
F Assimacopoulos-Jeannet et al.
Pflugers Archiv : European journal of physiology, 421(1), 52-58 (1992-05-01)
A beta-adrenergic agonist specific for brown adipose tissue, Ro 16-8714, was administered to control and obese insulin-resistant fa/fa rats and glucose utilisation measured in brown adipose tissue using the euglycaemic hyperinsulinaemic clamp combined with the injection of 2-deoxyglucose. Treatment with
Michail S Davidoff et al.
Histochemistry and cell biology, 124(3-4), 313-323 (2005-07-30)
Catecholamines play functional roles in the mature and developing mammalian testis but the cell types responsible for their local synthesis are still controversially discussed. Here, we demonstrate that four enzymes involved in the biosynthesis of catecholamines, namely, tyrosine hydroxylase (TH)