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50654-94-9

50654-94-9 structure
50654-94-9 structure

Name 2-[(tert-Butoxycarbonyl)amino]-3-(1H-imidazol-4-yl)propanoic acid
Synonyms N-(tert-Butoxycarbonyl)-D-histidine
BOC-D-HIS-OH
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-D-histidine
BOC-D-HISTIDINE
MFCD00037851
D-Histidine, N-[(1,1-dimethylethoxy)carbonyl]-
N(a)-Boc-D-histidine
Boc-D-histidine acid
Nalpha-BOC-D-Histidine
N(alpha)-Boc-D-histidine
Description (tert-Butoxycarbonyl)-D-histidine is a histidine 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 522.2±45.0 °C at 760 mmHg
Melting Point 193-197ºC
Molecular Formula C11H17N3O4
Molecular Weight 255.270
Flash Point 269.6±28.7 °C
Exact Mass 255.121902
PSA 104.31000
LogP 0.58
Vapour Pressure 0.0±1.4 mmHg at 25°C
Index of Refraction 1.542
Storage condition Store at 0-5°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
Safety Phrases 24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933290090
HS Code 2933290090
Summary 2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%