Ac-D-Phe-OH

Modify Date: 2024-01-02 11:57:56

Ac-D-Phe-OH Structure
Ac-D-Phe-OH structure
 Common Name Ac-D-Phe-OH
CAS Number 10172-89-1 Molecular Weight 207.226
Density 1.2±0.1 g/cm3 Boiling Point 453.9±38.0 °C at 760 mmHg
Molecular Formula C11H13NO3 Melting Point 167ºC
MSDS Chinese USA Flash Point 228.3±26.8 °C

 Use of Ac-D-Phe-OH


N-Acetyl-D-phenylalanine is a phenylalanine derivative[1].

 Names

Name N-acetyl-D-phenylalanine
Synonym More Synonyms

 Ac-D-Phe-OH Biological Activity

Description N-Acetyl-D-phenylalanine is a phenylalanine 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):1793-807.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 453.9±38.0 °C at 760 mmHg
Melting Point 167ºC
Molecular Formula C11H13NO3
Molecular Weight 207.226
Flash Point 228.3±26.8 °C
Exact Mass 207.089539
PSA 66.40000
LogP 0.78
Vapour Pressure 0.0±1.2 mmHg at 25°C
Index of Refraction 1.548
Storage condition −20°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924299090

 Synthetic Route

 Customs

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles25

More Articles
Peptide synthesis catalyzed by an antibody containing a binding site for variable amino acids.

Science 265 , 234, (1994)

Monoclonal antibodies, induced with a phosphonate diester hapten, catalyzed the coupling of p-nitrophenyl esters of N-acetyl valine, leucine, and phenylalanine with tryptophan amide to form the corres...

Studies on the mechanism for renal elimination of N-acetylphenylalanine: its pathophysiologic significance in phenylketonuria.

J. Lab. Clin. Med. 105(1) , 132-8, (1985)

To elucidate the mechanism and biologic significance of urinary occurrence of N-acetylphenylalanine in phenylketonuria, the metabolic fate of N-acetylphenylalanine was studied in rats. In vivo and in ...

Molecular dynamics (MD) simulations for the prediction of chiral discrimination of N-acetylphenylalanine enantiomers by cyclomaltoheptaose (beta-cyclodextrin, beta-CD) based on the MM-PBSA (molecular mechanics-Poisson-Boltzmann surface area) approach.

Carbohydr. Res. 339(11) , 1961-6, (2004)

Molecular dynamics (MD) simulations were performed for the prediction of chiral discrimination of N-acetylphenylalanine enantiomers by cyclomaltoheptaose (beta-cyclodextrin, beta-CD). Binding free ene...

 Synonyms

D-Phenylalanine, N-acetyl-
N-Acetyl-D-phenylalanine
MFCD00002664
Acetyl-D-Phenylalanine
(2R)-2-acetamido-3-phenylpropanoic acid
Ac-D-Phe-OH
EINECS 233-447-7
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