CAS 10172-89-1|Ac-D-Phe-OH

Introduction:Basic information about CAS 10172-89-1|Ac-D-Phe-OH, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameAc-D-Phe-OH
CAS Number10172-89-1Molecular Weight207.226
Density1.2±0.1 g/cm3Boiling Point453.9±38.0 °C at 760 mmHg
Molecular FormulaC11H13NO3Melting Point167ºC
MSDSChineseUSAFlash Point228.3±26.8 °C

Names

NameN-acetyl-D-phenylalanine
SynonymMore Synonyms

Ac-D-Phe-OH BiologicalActivity

DescriptionN-Acetyl-D-phenylalanine is a phenylalanine derivative[1].
Related CatalogResearch Areas >>OthersSignaling Pathways >>Others >>Others
In VitroAmino 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

Density1.2±0.1 g/cm3
Boiling Point453.9±38.0 °C at 760 mmHg
Melting Point167ºC
Molecular FormulaC11H13NO3
Molecular Weight207.226
Flash Point228.3±26.8 °C
Exact Mass207.089539
PSA66.40000
LogP0.78
Vapour Pressure0.0±1.2 mmHg at 25°C
Index of Refraction1.548
InChIKeyCBQJSKKFNMDLON-SNVBAGLBSA-N
SMILESCC(=O)NC(Cc1ccccc1)C(=O)O
Storage condition−20°C

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard CodesXi
RIDADRNONH for all modes of transport
WGK Germany3
HS Code2924299090

Customs

HS Code2924299090
Summary2924299090. 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

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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
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