Boc-Asp-OH

Modify Date: 2024-01-02 10:29:58

Boc-Asp-OH Structure
Boc-Asp-OH structure
Common Name Boc-Asp-OH
CAS Number 13726-67-5 Molecular Weight 353.327
Density 1.3±0.1 g/cm3 Boiling Point 609.3±55.0 °C at 760 mmHg
Molecular Formula C15H19N3O7 Melting Point 116-118 °C(lit.)
MSDS Chinese USA Flash Point 322.3±31.5 °C

 Use of Boc-Asp-OH


Boc-Asp-OH is an aspartic acid derivative[1].

 Names

Name Boc-Asp-OH
Synonym More Synonyms

 Boc-Asp-OH Biological Activity

Description Boc-Asp-OH is an aspartic acid 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.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 609.3±55.0 °C at 760 mmHg
Melting Point 116-118 °C(lit.)
Molecular Formula C15H19N3O7
Molecular Weight 353.327
Flash Point 322.3±31.5 °C
Exact Mass 353.122314
PSA 112.93000
LogP 2.05
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.550

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
Risk Phrases R20/21/22
Safety Phrases 26-36
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924199090

 Synthetic Route

 Customs

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%

 Articles1

More Articles
Aspartic acid-based modified PLGA–PEG nanoparticles for bone targeting: In vitro and in vivo evaluation

Acta Biomater. 10(11) , 4583-96, (2014)

Bone targeting NPs comprised of dendritic trimer of aspartic acid functionalized PLGA-PEG copolymers could be the foundation for hydrophobic-drug therapies.

 Synonyms

(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)succinic acid
EINECS 237-294-7
tert-butyloxycarbonyl-L-aspartic acid
BOC-ASP
L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-
Boc-L-aspartic acid
L-Asparagine, N-[(1,1-dimethylethoxy)carbonyl]-, 4-nitrophenyl ester
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-aspartic acid
BOC-L-ASP
N-t-butyloxycarbonyl-L-aspartic acid
BOC-ASPARTIC ACID
N-BOC-L-aspartic acid
L-Asparagine, N2-((1,1-dimethylethoxy)carbonyl)-, 4-nitrophenyl ester
N-Boc-aspartic acid
N-tert-Butoxycarbonyl-L-aspartic acid
tert-Butoxycarbonyl-L-aspartic acid
N-(tert-Butoxycarbonyl)-L-aspartic Acid
t-butoxycarbonyl-L-aspartic acid
Boc-L-Aspatic Acid
N-Boc-L-Asp-benzyl ester
MFCD00037279
N2-((1,1-Dimethylethoxy)carbonyl)-L-asparagine, 4-nitrophenyl ester
N-BOC-1-ASPARTICACID
4-Nitrophenyl N-(tert-butoxycarbonyl)-L-asparaginate
N-tert-Butyloxycarbonyl-L-aspartic acid
BOC-L-ASP-OH
Boc-D-Asp-OH
4-Nitrophenyl N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-asparaginate
BOC-L-Aspatic
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