H-Phe-Val-OH structure
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Common Name | H-Phe-Val-OH | ||
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CAS Number | 3918-90-9 | Molecular Weight | 264.32000 | |
Density | 1.166g/cm3 | Boiling Point | 509ºC at 760 mmHg | |
Molecular Formula | C14H20N2O3 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 261.7ºC |
Use of H-Phe-Val-OH(S)-2-((S)-2-Amino-3-phenylpropanamido)-3-methylbutanoic acid is a valine derivative[1]. |
Name | h-phe-val-oh |
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Synonym | More Synonyms |
Description | (S)-2-((S)-2-Amino-3-phenylpropanamido)-3-methylbutanoic acid is a valine derivative[1]. |
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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 |
Density | 1.166g/cm3 |
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Boiling Point | 509ºC at 760 mmHg |
Molecular Formula | C14H20N2O3 |
Molecular Weight | 264.32000 |
Flash Point | 261.7ºC |
Exact Mass | 264.14700 |
PSA | 92.42000 |
LogP | 1.87300 |
Index of Refraction | 1.549 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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RIDADR | NONH for all modes of transport |
HS Code | 2924299090 |
~% H-Phe-Val-OH CAS#:3918-90-9 |
Literature: Sheehan,J.C.; Guziec,F.S. Journal of Organic Chemistry, 1973 , vol. 38, p. 3034 - 3040 |
~53% H-Phe-Val-OH CAS#:3918-90-9 |
Literature: Kircher, K.; Berndt, H.; Zahn, H. Liebigs Annalen der Chemie, 1980 , # 2 p. 275 - 284 |
~% H-Phe-Val-OH CAS#:3918-90-9 |
Literature: Sheehan,J.C.; Guziec,F.S. Journal of Organic Chemistry, 1973 , vol. 38, p. 3034 - 3040 |
~% H-Phe-Val-OH CAS#:3918-90-9 |
Literature: Sheehan,J.C.; Guziec,F.S. Journal of Organic Chemistry, 1973 , vol. 38, p. 3034 - 3040 |
~% H-Phe-Val-OH CAS#:3918-90-9 |
Literature: Oya, Masanao; Takahashi, Tomoko Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 9 p. 2705 - 2707 |
~% H-Phe-Val-OH CAS#:3918-90-9 |
Literature: Schnabel,E. et al. Justus Liebigs Annalen der Chemie, 1967 , vol. 707, p. 227 - 241 |
HS Code | 2924299090 |
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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% |
Reactions of an aromatic σ,σ-biradical with amino acids and dipeptides in the gas phase.
J. Am. Soc. Mass Spectrom. 21 , 1737-1752, (2010) Gas-phase reactivity of a positively charged aromatic σ,σ-biradical (N-methyl-6,8-didehydroquinolinium) was examined toward six aliphatic amino acids and 15 dipeptides by using Fourier transform ion c... |
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Phenyl radical-induced damage to dipeptides.
J. Org. Chem. 74 , 7724-7732, (2009) Laser-induced acoustic desorption (LIAD) incorporated with Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR) has been utilized to investigate phenyl radical-induced damage to dipept... |
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An NH3+...phenyl interaction in L-phenylalanyl-L-valine.
Acta Crystallogr. C 56 , 1496-1498, (2000) One of the amino H atoms of L-phenylalanyl-L-valine, C(14)H(20)N(2)O(3), participates in a rare secondary interaction in being accepted by the aromatic ring of the phenylalanine side chain. The phenyl... |
Phenylalanyl-valin |
phenylalanylvaline |
L-phenylalanyl-L-valine |
PHE-VAL |
L-Phe-L-Val |