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16937-99-8

16937-99-8 structure
16937-99-8 structure

Name Boc-D-Leucine monohydrate
Synonyms Boc- D -Leu-OH
N-(tert-Butoxycbonyl)-D-leucine Hydrate>
N-(tert-Butoxycbonyl)-D-leucine Hydrate
N-(tert-Butoxycarbonyl)-D-leucine
D-Leucine, N-[(1,1-dimethylethoxy)carbonyl]-, hydrate (1:1)
BOC-D-LEUCINE-OH
N-T-BOC-D-LEUCINE
N-tert-butoxycarbonyl-D-leucine
Boc-D-Leu-OH >= (TLC)
4-methyl-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]pentanoic acid hydrate
N-Boc-D-leucine Hydrate
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-D-leucine hydrate (1:1)
Boc-D-Leu-OH hydrate
N-(tert-Butoxycbonyl)-D-leucine monohydrate
(R)-2-((TERT-BUTOXYCBONYL)AMINO)-4-METHYLPENTANOIC ACID
Cfilzomib Impurity
BOC-D-LEUCINE
N-ALPHA-T-BOC-D-LEUCINE
BOC-D-LeuClne
Boc-D-leucine hydrate (HPLC)
Boc-D-Leu-OH&BOC-D-LEU
N-(tert-Butoxycarbonyl)-D-leucine hydrate (1:1)
N-(tert-Butoxycarbonyl)-D-leucine Hydrate
L-LEUCINE-5,5,5-D3, N-T-BOC DERIV.H20 98
N-Boc-D-leucine Boc-D-Leu-OH
N-(t-butyloxycarbonyl)-D-leucine
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-D-leucine
D-Leucine, N-[(1,1-diMethylethoxy)carbonyl]
BOC-D-Leucine monohydrate //BP
MFCD00038294
N-BOC-D-Leucine.H2O
Boc-D-Leu-OH·H2O Boc-D-Leucine Monohydrate
Boc-D-Leu-OH Hydrate
N-(TERT-BUTOXYCBONYL)-D-LEUCINE
BOC-D-LEU-OH
n-(tert-butoxcbonyl)-d-leucine
N-Boc-D-leucine hydrate
BOC-D-LEU-OH2O
BOC-D-Leucine monohydrate
BOC-D-Leucinemonohydrate
(2R)-2-(tert-butoxycbonylamino)-4-methyl-pentanoic acid
Boc-D-Leu-OH
(R)-Boc-2-amino-4-methylpentanoic acid hydrate
(2R)-4-methyl-2-[(2-methylpropan-2-yl)oxycbonylamino]pentanoic acid
N-TERT-BUTOXYCBONYL-D-LEUCINE 1-HYDRATE
n-boc-d-leucine
tert-butoxycarbonyl-D-leucine
eucine monohydrate
BOC-D-LEU
Boc-(R)-leucine
tert-Butoxycbonyl-D-leucine
Description (tert-Butoxycarbonyl)-D-leucine is a leucine 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 1.1±0.1 g/cm3
Boiling Point 356.0±25.0 °C at 760 mmHg
Melting Point 85-87ºC(lit.)
Molecular Formula C11H21NO4
Molecular Weight 231.289
Flash Point 169.1±23.2 °C
Exact Mass 231.147064
PSA 84.86000
LogP 2.51
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.461
Storage condition −20°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
Safety Phrases S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
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%
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