Name | fmoc-glu(otbu)-oh h2o |
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Synonyms |
Fmoc-L-GlutamicacidmonohydrateO-t-butylester
FMOC-L-GLUTAMIC ACID (OTBU) MONOHYDRATE FMOC-L-GLU(OTBU)-OH H2O FMOC-L-GLUTAMIC ACID-O-T-BUTYL ESTER MONOHYDRATE FMOC-L-GLU(TBU)-OH H2O FMOC-L-Glutamic acid-O-tert-butyl ester monohydrate FMOC-GLUTAMIC ACID(OTBU)-OH H2O L-Glutamic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 5-(1,1-dimethylethyl) ester, hydrate (1:1) Fmoc-L-Glu(otbu)-OH hydrate FMOC-GLU(OBUT) H2O (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid hydrate Fmoc-L-Glutamic acid-O-tert-butyl ester hydrate (2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-5-[(2-methyl-2-propanyl)oxy]-5-oxopentanoic acid hydrate (1:1) MFCD00150485 |
Description | (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid hydrate is a glutamic acid 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 |
Boiling Point | 633.5ºC at 760mmHg |
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Melting Point | 89-93ºC |
Molecular Formula | C24H29NO7 |
Molecular Weight | 443.490 |
Flash Point | 336.9ºC |
Exact Mass | 443.194397 |
PSA | 111.16000 |
LogP | 4.42680 |
Vapour Pressure | 6.39E-17mmHg at 25°C |
Storage condition | -20°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |