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284491

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

Name: (<I>R</I>)-(+)-2-Amino-3-phenyl-1-propanol
Brand: ALDRICH

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

Assay:

98%

Form:

solid

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Properties

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

Description

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363

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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Synthesis, Characterisation and In Vitro Permeation, Dissolution and Cytotoxic Evaluation of Ruthenium(II)-Liganded Sulpiride and Amino Alcohol.

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

Synthesis and activity of 2-oxoamides containing long chain beta-amino acids.

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

tRNAPhe and tRNAPro are the near-ultraviolet molecular targets triggering the growth delay effect.

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

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Global Trade Item Number

SKU	GTIN
284491-5G	04061833037904
284491-1G	04061826253496