H-Phe-ol

Modify Date: 2025-08-20 17:35:24

H-Phe-ol structure	Common Name	H-Phe-ol
	CAS Number	3182-95-4	Molecular Weight	151.206
	Density	1.1±0.1 g/cm3	Boiling Point	303.8±22.0 °C at 760 mmHg
	Molecular Formula	C₉H₁₃NO	Melting Point	92-94ºC
	MSDS	Chinese USA	Flash Point	137.5±22.3 °C
	Symbol	GHS05	Signal Word	Danger

Use of H-Phe-ol

L-(-)-Phenylalaninol is an alanine derivative[1].

Name	(2S)-2-amino-3-phenylpropan-1-ol
Synonym	More Synonyms

Description	L-(-)-Phenylalaninol is an alanine derivative[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
In Vitro	Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References	[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1093.

Density	1.1±0.1 g/cm3
Boiling Point	303.8±22.0 °C at 760 mmHg
Melting Point	92-94ºC
Molecular Formula	C₉H₁₃NO
Molecular Weight	151.206
Flash Point	137.5±22.3 °C
Exact Mass	151.099716
PSA	46.25000
LogP	0.77
Vapour Pressure	0.0±0.7 mmHg at 25°C
Index of Refraction	1.561
InChIKey	STVVMTBJNDTZBF-VIFPVBQESA-N
SMILES	NC(CO)Cc1ccccc1

H-Phe-ol MSDS(Chinese)

CHEMICAL IDENTIFICATION

RTECS NUMBER :: UA6900000

CHEMICAL NAME :: 1-Propanol, 2-amino-3-phenyl-, L-

CAS REGISTRY NUMBER :: 3182-95-4

LAST UPDATED :: 199712

DATA ITEMS CITED :: 2

MOLECULAR FORMULA :: C9-H13-N-O

MOLECULAR WEIGHT :: 151.23

WISWESSER LINE NOTATION :: Q1YZ1R -L

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD - Lethal dose

ROUTE OF EXPOSURE :: Oral

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: >1 gm/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: JMCMAR Journal of Medicinal Chemistry. (American Chemical Soc., Distribution Office Dept. 223, POB POB 57136, West End Stn., Washington, DC 20037) V.6- 1963- Volume(issue)/page/year: 11,854,1968

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intraperitoneal

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 76 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: JMCMAR Journal of Medicinal Chemistry. (American Chemical Soc., Distribution Office Dept. 223, POB POB 57136, West End Stn., Washington, DC 20037) V.6- 1963- Volume(issue)/page/year: 20,1578,1977

Symbol	GHS05
Signal Word	Danger
Hazard Statements	H314
Precautionary Statements	P280-P305 + P351 + P338-P310
Personal Protective Equipment	Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges
Hazard Codes	C: Corrosive;
Risk Phrases	R34
Safety Phrases	S24/25
RIDADR	UN 3259 8/PG 3
WGK Germany	3
RTECS	UA6900000
Hazard Class	8.0
HS Code	29221980

Precursor 9
CAS#:63-91-2 L-Phenylalanine CAS#:7524-50-7 Methyl L-phenyl... CAS#:2577-90-4 Methyl L-phenyl... CAS#:6372-14-1 (S)-Cbz-Phenyla...
CAS#:3182-93-2 H-Phe-OEt.HCl CAS#:59830-60-3 (S)-(-)-2-(Benz... CAS#:150-30-1 DL-Phenylalanine CAS#:2935-35-5 H-Phg-OH
CAS#:129397-83-7 Fmoc-Phe-ol
DownStream 10
CAS#:141403-49-8 (S)-2-((TERT-BU... CAS#:223600-53-1 1-[(2S)-1-hydro... CAS#:300-57-2 Allylbenzene CAS#:93-54-9 phenyl propanol
CAS#:1334326-63-4 5-benzyl-3-meth... CAS#:29802-26-4 (2S)-N1,N1-Dime... CAS#:82495-70-3 (S)-(-)-N-(3-PE... CAS#:90719-32-7 (S)-4-Benzyl-2-...
CAS#:2448-45-5 Z-D-Phe-OH CAS#:2323-36-6 1-[4-[2-[(4-chl...

HS Code	2922199090
Summary	2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Straightforward methodology for the enantioselective synthesis of benzo[a]- and indolo[2,3-a]quinolizidines.

J. Org. Chem. 72(14) , 5193-201, (2007)

An enantioselective two-step route to substituted benzo[a]- and indolo[2,3-a]quinolizidines has been developed. It consists of (i) a stereoselective cyclocondensation of a racemic or prochiral delta-o...

Direct high-performance liquid chromatographic separation of the enantiomers of an aromatic amine and four aminoalcohols using polysaccharide chiral stationary phases and acidic additive.

Chirality 19(8) , 647-53, (2007)

The HPLC enantiomeric separation of N-benzyl-alpha-methyl-benzylamine, phenylalaninol, tryptophanol, 2 (diphenylhydroxymethyl)pyrrolidine, and isoproterenol was accomplished in the normal-phase mode u...

Paracelsin; characterization by NMR spectroscopy and circular dichroism, and hemolytic properties of a peptaibol antibiotic from the cellulolytically active mold Trichoderma reesei. Part B.

Experientia 40 , 1189, (1984)

Paracelsin, a hemolytic and membrane active polypeptide antibiotic of the peptaibol class which is excreted by the mold Trichoderma reesei, was obtained by a simplified and rapid isolation procedure u...

Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN

Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN

Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN

Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100

Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101

Name: Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
Source: Broad Institute
Target: N/A
External Id: 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2

Name: Spectrum HTS for Inhibitors of Aerobactin Synthetase IucA
Source: 23265
Target: IucA Synthetase from hypervirulent Klebsiella pneumoniae hvKP1
External Id: IucA Pilot Assay Spectrum Library

Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity

Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity

Name: The chemical genetic matrix (CGM) dataset as reported in Wildenhain et al. (2015) Pre...
Source: 11924
Target: N/A
External Id: CGM data for Cell Systems paper Dec 2015

Total 94, Current Page 1 of 10

β-Anilinoethanol

HPH

(S)-(-)-2-amino-3-phenylpropan-1-ol

(S)-2-Amino-3-phenyl-1-propanol

(S)-2-Amino-3-phenylpropan-1-ol

(S)-2-amino-2-phenylpropan-1-ol

(S)-2-Amino-3-phenyl-propan-1-ol

N-(β-hydroxy)ethylaniline

L(-)-2-Amino-3-phenyl-1-propanol

2-(phenylamino)ethanol

EINECS 221-674-4

H-Phenylalaninol

(S)-(-)-2-Amino-3-phenyl-1-propanol

(S)-(-)-phenylalaninol

(2S)-2-amino-3-phenylpropanol

(2S)-2-Amino-3-phenyl-1-propanol

(-)-L-PHENYLALANINOL

(2S)-2-amino-3-phenylpropan-1-ol

L-phenylalaninol

(S)-β-Aminobenzenepropanol

phenylalaninol

2-amino-3-phenylpropan-1-ol

(S)-(−)-2-Amino-3-phenyl-1-propanol

N-(β-Hydroxyethyl)aniline

2-Amino-3-Phenyl-Propan-1-Ol

2-Anilinoethanol

H-Phe-ol

MFCD00004732

(±)-phenylethanolamine

N-2-hydroxyethylaniline

L-Phenylglycinol

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H-Phe-ol

Use of H-Phe-ol

Names

H-Phe-ol Biological Activity

Chemical & Physical Properties

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

Safety Information

Precursor & DownStream

Customs

Articles17

H-Phe-olBioassay

Synonyms

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