Boc- Gly- OH
Also known as N-(tert-Butoxycarbonyl)glycine, N-Boc-glycine, t-Butoxycarbonylglycine
- CAS number
- 4530-20-5
- Molecular formula
- C7H13NO4
- Molecular weight
- 175.2 g/mol
- Catalogue number
- OS-18586
- Purity
- 98 %
- Grade
- Industrial, Pharmaceutical (IP/BP/USP/EP), Agricultural, Technical
- Form
- Powder
- Packing
- 25 kg, 25 kg
₹900 per kg
Documents
- Certificate of analysis (COA) On request
- Safety data sheet (MSDS) On request
Specifications
| CAS number | 4530-20-5 |
|---|---|
| Molecular formula | C7H13NO4 |
| Molecular weight | 175.2 g/mol |
| IUPAC name | 2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid |
| InChIKey | VRPJIFMKZZEXLR-UHFFFAOYSA-N |
| SMILES | CC(C)(C)OC(=O)NCC(=O)O |
| PubChem CID | 78288 |
| Physical form | Powder |
|---|---|
| Appearance | Off-White Powder |
| Solubility | Soluble in Organic Solvents |
| Purity | 98 % |
|---|---|
| Grade | Industrial, Pharmaceutical (IP/BP/USP/EP), Agricultural, Technical |
| Packaging size | 25 kg, 25 kg |
|---|---|
| Packaging type | Drum, Bag |
Description and applications
Synonums : Boc-glycine Boc-glycine is widely utilized in research focused on:
- Peptide Synthesis: It serves as a protecting group for amino acids during the synthesis of peptides, allowing for selective reactions without affecting other functional groups.
- Drug Development: In pharmaceutical research, Boc-glycine is used to modify drug candidates, enhancing their stability and bioavailability, which is crucial for developing effective medications.
- Bioconjugation: This compound is employed in bioconjugation techniques to link biomolecules, such as proteins and antibodies, facilitating the creation of targeted therapies and diagnostics.
- Polymer Chemistry: It plays a role in the synthesis of polyamides and other polymers, contributing to materials with specific properties for applications in coatings and adhesives.
- Analytical Chemistry: Boc-glycine is utilized in chromatography and mass spectrometry as a derivatizing agent, improving the detection and analysis of various compounds.
Applications
- Industrial
- Pharmaceutical
- It serves as a protecting group for amino acids during the synthesis of peptides
More protected amino acids
All 21 protected amino acids-
BOC-D- Phenyl glycine
(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid, Boc-D-Phg-OH
CAS 33125-05-2 C13H17NO4 99 % -
N-BOC-D- Phenyl glycinol
1,1-Dimethylethyl N-((1R)-2-hydroxy-1-phenylethyl)carbamate, (R)-N-(tert-Butoxycarbonyl)-2-phenylglycinol
CAS 102089-74-7 C13H19NO3 99 % -
BOC- Gly- Ome
N-Boc-glycine Methyl Ester, N-(tert-Butoxycarbonyl)glycine methyl ester
CAS 31954-27-5 C8H15NO4 99 % -
Boc- L- Alanine
tert-butoxycarbonylalanine, t-BA amino acid
CAS 15761-38-3 C8H15NO4 99 % -
N-BOC-L- Hydroxy proline
Boc-Hyp-OH, N-Boc-trans-4-hydroxy-L-proline
CAS 13726-69-7 C10H17NO5 7 % -
N-BOC-L- phenyl alanine
N-(tert-Butoxycarbonyl)-L-phenylalanine, N-t-Butyloxycarbonyl-L-phenylalanine
CAS 13734-34-4 C14H19NO4 99 %
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