Boc- D -His-OH

Names

[ Name ]:
Boc- D -His-OH

[Synonym ]:
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

Biological Activity

[Description]:

(tert-Butoxycarbonyl)-D-histidine is a histidine 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 ]:
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

MSDS

Click to get detail MSDS

Safety Information

[ 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

Customs

[ 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%