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284491

Sigma-Aldrich

(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
Beilstein:
2208239
EC Number:
226-086-1
MDL number:
MFCD00064298
UNSPSC Code:
12352116
PubChem Substance ID:
24857160
NACRES:
NA.22

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

SMILES string

N[C@@H](CO)Cc1ccccc1

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

InChI key

STVVMTBJNDTZBF-SECBINFHSA-N

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

284491-1G:
284491-5G:
284491-BULK:
284491-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
SHBN0249
SHBF1731V
SHBD7181V
67896APV
67896AP

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W W Mak et al.
Canadian journal of biochemistry, 58(12), 1421-1429 (1980-12-01)
The activities of a range of phenylalaninol-related compounds on capping of concanavalin A and induction of rounding of Chinese hamster ovary tsHl cells, as well as on the fluidity of phosphatidylcholine-cholesterol (1:1) liposomes, have been examined. These compounds include phenylalaninol
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
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
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
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
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