H-Phe-ol

Modify Date: 2024-01-01 18:12:13

H-Phe-ol Structure
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
GHS05
Signal Word Danger

 Use of H-Phe-ol


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

 Names

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

 H-Phe-ol Biological Activity

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

 Chemical & Physical Properties

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

 Toxicological Information

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

 Safety Information

Symbol GHS05
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

 Customs

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%

 Articles17

More Articles
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...

 Synonyms

Ethanol, 2- (phenylamino)-
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
Aniline, N-(β-hydroxyethyl)-
Ethanol, 2-(phenylamino)-
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
Benzenepropanol, β-amino-, (βS)-
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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