Boc-Gly-OH

Modify Date: 2024-01-01 21:19:25

Boc-Gly-OH Structure
Boc-Gly-OH structure
Common Name Boc-Gly-OH
CAS Number 4530-20-5 Molecular Weight 175.182
Density 1.2±0.1 g/cm3 Boiling Point 315.9±25.0 °C at 760 mmHg
Molecular Formula C7H13NO4 Melting Point 86-89 °C(lit.)
MSDS USA Flash Point 144.9±23.2 °C

 Use of Boc-Gly-OH


Boc-Glycine is a Glycine (HY-Y0966) derivative[1].

 Names

Name t-Butoxycarbonylglycine
Synonym More Synonyms

 Boc-Gly-OH Biological Activity

Description Boc-Glycine is a Glycine (HY-Y0966) 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 1.2±0.1 g/cm3
Boiling Point 315.9±25.0 °C at 760 mmHg
Melting Point 86-89 °C(lit.)
Molecular Formula C7H13NO4
Molecular Weight 175.182
Flash Point 144.9±23.2 °C
Exact Mass 175.084457
PSA 75.63000
LogP 0.75
Vapour Pressure 0.0±1.4 mmHg at 25°C
Index of Refraction 1.460
Storage condition -20°C
Water Solubility soluble

 Safety Information

Personal Protective Equipment dust mask type N95 (US);Eyeshields;Faceshields;Gloves
Hazard Codes Xi:Irritant
Risk Phrases R41
Safety Phrases S26-S36/37/39-S39
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
Hazard Class 6.1
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%

 Articles9

More Articles
In situ fabrication of cleavable peptide arrays on polydimethylsiloxane and applications for kinase activity assays.

Anal. Chim. Acta 865 , 53-9, (2015)

Polydimethylsiloxane (PDMS) is widely used for microfabrication and bioanalysis; however, its surface functionalization is limited due to the lack of active functional groups and incompatibility with ...

Accumulation of cell-penetrating peptides in large unilamellar vesicles: A straightforward screening assay for investigating the internalization mechanism.

Biopolymers 104 , 533-43, (2015)

The internalization of cell-penetrating peptides (CPPs) into liposomes (large unilamellar vesicles, LUVs) was studied with a rapid and robust procedure based on the quenching of a small fluorescent pr...

Optimization of the Ugi reaction using parallel synthesis and automated liquid handling.

J. Vis. Exp. (21) , doi:10.3791/942, (2008)

The optimization of a Ugi reaction involving the mixing of furfurylamine, benzaldehyde, boc-glycine and t-butylisocyanide is described. Triplicate runs of 48 parallel experiments are reported, varying...

 Synonyms

N-(tert-Butoxycarbonyl)glycin
Glycine, N-[(1,1-dimethylethoxy)carbonyl]-
Boc-glycine
N-Boc-protected glycine
n-boc-glycine
boc-gly
N-(tert-butoxycarbonyl)glycine
Boc-Gly-OH
MFCD00002690
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}glycine
N-Boc-L-glycine
2-((tert-Butoxycarbonyl)amino)acetic acid
({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)acetic acid
Glycine, N-carboxy-, N-tert-butyl ester
N-Boc glycine
EINECS 224-864-5
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