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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 Information

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Certificates of Analysis (COA)

Lot/Batch Number
SHBN0249
SHBF1731V
SHBD7181V
67896APV
67896AP

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B Weiss et al.
Research communications in chemical pathology and pharmacology, 62(1), 113-123 (1988-10-01)
An amino acid derivative, leucinethiol, was reported to be a strong inhibitor of aminopeptidase activity. In order to obtain selective inhibitors of various brain aminopeptidases, we tested the inhibition by amino acid analogs of brain aminopeptidase activity. In particular, we
H Hashizume et al.
Chemical & pharmaceutical bulletin, 40(11), 3113-3114 (1992-11-01)
The effects of phenylalaninol (D-isomer) on gastric acid secretion and gastric ulcer were studied in rats. The compound reduced the gastric acid secretion stimulated by intracisternal thyrotropin releasing hormone and intravenous 2-deoxy-D-glucose, but not that stimulated by subcutaneous carbachol or
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
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
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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