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5354-94-9

5354-94-9 structure
5354-94-9 structure

Name N-α-BENZOYL-L-HISTIDINE
Synonyms BENZOYL-L-HISTIDINE MONOHYDRATE
EINECS 226-332-8
BZ-HIS-OH
N-alpha-Benzoyl-L-Histidine
N-Benzoyl-L-Histidine
benzoyl-His
MFCD00037850
Histidine, N-benzoyl-
N-Benzoyl-Histidine
BZO-HIS-OH
Benzoylhistidine
BENZOYL-L-HISTIDINE
BENZOYL-HIS-OH
(S)-2-benzoylamino-3-(1H-imidazol-4-yl)propanoic acid
BZ-HISTIDINE
N-Benzoylhistidine
Description Benzoyl-L-histidine Monohydrate 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 1.4±0.1 g/cm3
Boiling Point 662.3±50.0 °C at 760 mmHg
Molecular Formula C13H13N3O3
Molecular Weight 259.261
Flash Point 354.3±30.1 °C
Exact Mass 259.095703
PSA 95.08000
LogP -0.04
Vapour Pressure 0.0±2.1 mmHg at 25°C
Index of Refraction 1.631
Storage condition −20°C
WGK Germany 3
HS Code 2933290090

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5354-94-9 structure

5354-94-9

Literature: Tetrahedron Asymmetry, , vol. 19, # 3 p. 273 - 278

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5354-94-9 structure

5354-94-9

Literature: Biochemical Preparations, , vol. 4, p. 46,50

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5354-94-9 structure

5354-94-9

Literature: Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, , vol. 108, p. 53
Precursor  3

DownStream  2

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%