Fmoc-Hyp(tBu)-OH

Names

[ Name ]:
Fmoc-Hyp(tBu)-OH

[Synonym ]:
Fmoc-Hyp(tBu)
(2S,4R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-(tert-butoxy)pyrrolidine-2-carboxylic acid
Fmoc-Hyp(OtBu)-OH
FMOC-O-T-BUTYL-L-HYDROXYPROLINE
FMOC-HYDROXYPROLINE(TBU)-OH
FMOC-L-HYP(TBU)-OH
Fmoc-4-tert-butoxy-L-proline
(4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[(2-methyl-2-propanyl)oxy]-L-proline
FMOC-O-T-BUTYL-L-4-HYDROXYPROLINE
1,2-Pyrrolidinedicarboxylic acid, 4-(1,1-dimethylethoxy)-, 1-(9H-fluoren-9-ylmethyl) ester, (2S,4R)-
Fmoc-Hyp(tBu)-OH
MFCD00065655
FMOC-HYP(TBU)-OHMIN
FMOC-HYP(BUT)-OH

Biological Activity

[Description]:

Fmoc-Hyp(tBu)-OH is a proline derivative[1].

[Related Catalog]:

Research Areas >> Others

Signaling 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):1793-1144.

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
578.6±50.0 °C at 760 mmHg

[ Melting Point ]:
-63ºC

[ Molecular Formula ]:
C₂₄H₂₇NO₅

[ Molecular Weight ]:
409.475

[ Flash Point ]:
303.7±30.1 °C

[ Exact Mass ]:
409.188934

[ PSA ]:
76.07000

[ LogP ]:
3.60

[ Vapour Pressure ]:
0.0±1.7 mmHg at 25°C

[ Index of Refraction ]:
1.619

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
22-24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

Non-covalent photo-patterning of gelatin matrices using caged collagen mimetic peptides.

Macromol. Biosci. 15(1) , 52-62, (2015)

To address the downside of conventional photo-patterning which can alter the chemical composition of protein scaffolds, we developed a non-covalent photo-patterning strategy for gelatin (denatured col...