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34404-28-9

34404-28-9 structure
34404-28-9 structure

Name (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanedioic acid
Synonyms Boc-Glu-COOH
N-(Tert-Butoxycarbonyl)-D-Glutamic Acid
L-Glutamic acid, N-[(1,1-dimethylethoxy)carbonyl]-
N-(tert-Butoxycarbonyl)-L-glutamic Acid
Boc-L-Glutamicacid
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-glutamic acid
Boc-L-Glu-OH
N-Boc-L-glutamic Acid
Boc-D-glutamic acid
(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)pentanedioic acid
Boc-D-Glu-OH
N-Boc-D-glutamic Acid
Boc-L-Glutamic acid
N-BOC-L-Glu
N-Boc-D-Glu
MFCD00190790
Boc-Glu-OH
(R)-2-((tert-Butoxycarbonyl)amino)pentanedioic acid
Description BOC-D-GLU-OH is a glutamic acid 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):1793-1144.

Density 1.3±0.1 g/cm3
Boiling Point 435.9±35.0 °C at 760 mmHg
Melting Point 108 °C(dec.)
Molecular Formula C10H17NO6
Molecular Weight 247.245
Flash Point 217.4±25.9 °C
Exact Mass 247.105591
PSA 112.93000
LogP 0.34
Vapour Pressure 0.0±2.2 mmHg at 25°C
Index of Refraction 1.493
Storage condition Store at RT.
Hazard Codes Xi
HS Code 2924199090
HS Code 2924199090
Summary 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%