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Merck
CN

284491

(R)-(+)-2-Amino-3-phenyl-1-propanol

98%

Synonym(s):

D-Phenylalaninol

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About This Item

Linear Formula:
C6H5CH2CH(NH2)CH2OH
CAS Number:
5267-64-1
Molecular Weight:
151.21
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
24857160
EC Number:
226-086-1
Beilstein/REAXYS Number:
2208239
MDL number:
MFCD00064298

Key Documents

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Product Name

(R)-(+)-2-Amino-3-phenyl-1-propanol, 98%

InChI key

STVVMTBJNDTZBF-SECBINFHSA-N

InChI

1S/C9H13NO/c10-9(7-11)6-8-4-2-1-3-5-8/h1-5,9,11H,6-7,10H2/t9-/m1/s1

SMILES string

N[C@@H](CO)Cc1ccccc1

assay

98%

form

solid

optical activity

[α]/D +22.8°, c = 1.2 in 1 M HCl

mp

93-95 °C (lit.)

functional group

amine
hydroxyl
phenyl

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
SHBN0249
SHBF1731V
SHBD7181V
67896APV
67896AP

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Gretta C M'bitsi-Ibouily et al.
Scientific reports, 9(1), 4146-4146 (2019-03-13)
Sulpiride (SPR) is a selective antagonist of central dopamine receptors but has limited clinical use due to its poor pharmacokinetics. The aim of this study was to investigate how metal ligation to SPR may improve its solubility, intestinal permeability and
G P Zecchini et al.
Archiv der Pharmazie, 328(9), 673-676 (1995-09-01)
The synthesis and the biological activity towards human neutrophils of some N-formyl-Met-Leu-Phe-OMe analogues containing (S)-phenylalaninol (Pheol) or its derivatives in place of the native phenylalanine are reported. While the analogue containing Pheol (4) was found to be devoid of significant
M O Blondel et al.
Biochemical and biophysical research communications, 150(3), 979-986 (1988-02-15)
The illumination of Escherichia coli cells with UVA light, 320 nm less than or equal to lambda less than or equal to 380 nm, triggers a transient growth and division delay. The built-in 4-thiouridine chromophore which absorbs light at 340
W W Mak et al.
Canadian journal of biochemistry, 58(9), 737-744 (1980-09-01)
This study describes a rounding reaction induced in mammalian cells by the addition of phenylalaninol. In the Chinese hamster ovary tsH1 line the rounding occurred rapidly with a half time of 1 min at 25 mM phenylalaninol. After the removal
Violetta Constantinou-Kokotou et al.
Journal of peptide science : an official publication of the European Peptide Society, 11(7), 431-435 (2005-01-07)
2-Oxoamides based on long chain beta-amino acids were synthesized. 1-Benzyl substituted long chain amines, needed for such synthesis, were synthesized starting from Boc-phenylalaninol. The oxidative conversion of a phenyl group to a carboxyl group was used as the key transformation
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