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H1754

Supelco

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:
7568-93-6
Molecular Weight:
137.18
Beilstein:
971222
EC Number:
231-469-1
MDL number:
MFCD00008137
UNSPSC Code:
41116107
PubChem Substance ID:
329815178
Pricing and availability is not currently available.

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

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Product No.
Description
Pricing

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P261 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
069F3669
066H3616
036H2514
096H3607
081F7701

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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
M Landi et al.
Biochemical pharmacology, 44(4), 665-672 (1992-08-18)
[3H]Dihydroalprenolol ([3H]DHA) specific binding (determined by the difference in the presence and absence of 20 microM (-)isoprenaline) to rat colon membranes was saturable (Bmax = 39.6 fmol/mg protein), of high affinity (Kd = 0.87 nM) and stereospecific (IC50 330 and
Erkan Karakas et al.
Nature, 475(7355), 249-253 (2011-06-17)
Since it was discovered that the anti-hypertensive agent ifenprodil has neuroprotective activity through its effects on NMDA (N-methyl-D-aspartate) receptors, a determined effort has been made to understand the mechanism of action and to develop improved therapeutic compounds on the basis
C G Ziegler et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(37), 15879-15884 (2009-09-01)
Peptide analogues targeting various neuropeptide receptors have been used effectively in cancer therapy. A hallmark of adrenocortical tumor formation is the aberrant expression of peptide receptors relating to uncontrolled cell proliferation and hormone overproduction. Our microarray results have also demonstrated
K M Buller et al.
Neuropharmacology, 49(2), 230-242 (2005-07-05)
In opiate addicts or patients receiving morphine treatment, it has been reported that the immune system is often compromised. The mechanisms responsible for the adverse effects of opioids on responses to infection are not clear but it is possible that
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