CAS 3182-95-4|H-Phe-ol

Introduction：Basic information about CAS 3182-95-4|H-Phe-ol, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. H-Phe-ol BiologicalActivity
3. Chemical & Physical Properties
4. Toxicological Information
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATA
ACUTE TOXICITY DATA
5. Safety Information
6. Customs
7. Articles17
8. Synonyms

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	ChineseUSA	Flash Point	137.5±22.3 °C
Symbol	GHS05	Signal Word	Danger

Names

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

H-Phe-ol BiologicalActivity

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

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
InChIKey	STVVMTBJNDTZBF-VIFPVBQESA-N
SMILES	NC(CO)Cc1ccccc1

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
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

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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