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35897-34-8

35897-34-8 structure
35897-34-8 structure

Name N-BOC-D-Arginine hydrochloride
Synonyms BOC-ARG-OH.HCI
BOC-ARGININE
Nalpha L
N^a-Boc-L-ginine hydrochloride
Boc-q-OH.HCl.H2O
Nalpha-(tert-Butoxycbonyl)-L-ginine Hydrochloride
n-boc-L-ginine hydrochloride
N-ALPHA-(TERT-BUTOXYCBONYL)-L-GININEHCL
Boc-Arg-OH hydrochloride
N-ALPHA-BOC-L-GININE HYDROCHLORIDE
Boc-Arg-OH.HCl.H2O
BOC-D-arginine hydrochloride
Boc-g-OH·HCl·H2O N-α-Boc-L-ginine hydrochloride Monohydrate
N-ALPHA-T-BUTYLOXYCBONYL-L-GININE MONOHYDRATE HYDROCHLORIDE
Nα-(tert-Butoxycbonyl)-L-ginineHydrochlorideMonohydrate>
(tert-Butoxycbonyl)-L-ginine hydrochloride
Boc-L-g HCl
Boc-Arg.HCl.H2O
L-ginine, N2-[(1,1-diMethylethoxy)carbonyl]-, Monohydrochloride
BOC-L-ARGININE
Nalpha-(tert-Butoxycbonyl)-L-ginine Hydrochloride Monohydrate
Boc-L-ginine HCl
nα-boc-l-ginine hydrochloride
Nα-(tert-Butoxycarbonyl)-L-arginine Hydrochloride Monohydrate
N-BOC-D-Argininehydrochloride
(S)-2-((tert-Butoxycarbonyl)amino)-5-guanidinopentanoic acid hydrochloride
Boc-L-ginine hydrochloride
Boc-g-OH hydrochloride >= (TLC)
Boc-L-Arg-OH*HCl
N-ALPHA-(TERT-BUTOXYCBONYL)-L-GININE HYDRCHLORIDE
Boc-g-HCl
Nα-Boc-L-ginine hydrochloride hydrate (HPLC)
Nalpha-Boc-L-ginine Hydrochloride Boc-g-OH.HCl
Nα-Boc-L-ginine hy
BOC-ARGININE HCL
N-(Diaminomethylene)-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-ornithine hydrochloride (1:1)
Boc-L-g-OH*H2O*HCl
Nalpha-(tert-butoxycbonyl)-L-alanine hydrochloride
BOC-G-OH.HCLN-ALPHA BOC-L GININE HYDRO CHLORIDE
N-BOC-L-ginine hydrochloride //BP
(S)-2-((tert-Butoxycbonyl)amino)-5-guanidinopentanoic acid hydrochloride
Nα-Boc-L-arginine Hydrochloride Monohydrate
Boc-Arg-OHhydrochloride
Boc-g-OH·H2O·HCl
N-ALPHA-T-BUTOXYCBONYL-L-GININE
N-ALPHA-T-BOC-L-G
Boc-L-arginine HCl
EINECS 237-295-2
Boc-Arg-OH&BOC-L-ARG-OH HCL
BOC-L-G-OH HCL
Boc-g.HCl.H2O
BOC-L-GININE
N-(tert-Butoxycarbonyl)-L-arginine hydrochloride (1:1)
N-T-BOC-L-GININE
BOC-G-OH.HCI
Boc-L-g·HCl
BOC-GININE HCL
BOC-ARG-OH HCL
Boc-g-OHHC
Boc-Arg-OHHC
NALPHA-(TERT-BUTOXYCBONYL)-L-GININE
L-Ornithine, N-(diaminomethylene)-N-[(1,1-dimethylethoxy)carbonyl]-, hydrochloride (1:1)
BOC-ARG-OH
N-TERT-BUTOXYCBONYL-L-GININE
BOC-G-OH HYDROCHLORIDE
BOC-G-OH HCL
Nα-(tert-Butoxycbonyl)-L-ginine
Boc-g-OH·HCl·H2O
BOC-GININE
Boc-Arg-OH·HCl Monohydrate
BOC-L-GININE HYDROCHLORIDE H20
Boc-Arg*HCl
N-ALPHA-TERT-BUTYLOXYCBONYL-L-GININE 1-HYDRATE HYDROCHLORIDE
Nα-Boc-L-ginine hydrochloride hydrate
Boc-Arg hydrochloride
Boc-Arg-OH.H2O.HCl
N-tert-Butoxycbonyl-L-ginine hydrochloride
Boc-g-OH. HCl (Boc-L-ginine Hcl)
N2-Boc-L-ginine Hydrochloride
Nα-Boc-L-ginine
BOC-G-OH
N-.ALPHA.-BOC-L-GININE HYDROCHLORIDE MONOHYDRATE
MFCD00042632
Description (tert-Butoxycarbonyl)-L-arginine hydrochloride is an arginine 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 1.28g/cm3
Molecular Formula C11H23ClN4O4
Molecular Weight 310.778
Flash Point >230 °F
Exact Mass 310.140778
PSA 137.53000
LogP 2.61140
Index of Refraction -8 ° (C=2, H2O)
Storage condition -15°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
Precursor  0

DownStream  3

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