Boc-Dap-OH
≥98.0% (TLC)
Manufacturer: Sigma Aldrich
CAS Number: 73259-81-1
Synonym(S): (S)-2-[(tert-Butoxycarbonyl)amino]-3-aminopropionic acid, (S)-3-Amino-2-(tert-butoxycarbonyl)aminopropionic acid, (S)-3-Amino-2-(tert-butoxycarbonylamino)propanoic acid, 3-Amino-(tert-butoxycarbonyl)-L-alanine, Nα-BOC-(S)-β-aminoalanine, Nα-Boc-L-β-aminoalanine, N2-(tert-Butoxycarbonyl)-(S)-2,3-diaminopropionic acid, N2-tert-Butoxycarbonyl-L-2,3-diaminopropionic acid, Nα-Boc-L-2,3-diaminopropionic acid, Boc-Dpr-OH
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | 15402-1-G | In Stock | ₹ 5,737.25 |
| 5 G | 15402-5-G | In Stock | ₹ 21,888.15 |
15402 - 1 G
In Stock
Quantity
1
Base Price: ₹ 5,737.25
GST (18%): ₹ 1,032.705
Total Price: ₹ 6,769.955
Quality Level
100
Assay
≥98.0% (TLC)
form
solid
optical activity
[α]20/D +5.5±1°, c = 1% in methanol: water (1:1)
reaction suitability
reaction type: Boc solid-phase peptide synthesis
impurities
~3% water
mp
210 °C (dec.)
application(s)
peptide synthesis
SMILES string
CC(C)(C)OC(=O)N[C@@H](CN)C(O)=O
InChI
1S/C8H16N2O4/c1-8(2,3)14-7(13)10-5(4-9)6(11)12/h5H,4,9H2,1-3H3,(H,10,13)(H,11,12)/t5-/m0/s1
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Chem-Impex International, Inc. Na-Boc-L-2,3-diaminopropionic acid | 73259-81-1 | MFCD00236843 | 25G | Chem-Impex International, Inc. | ₹ 30,066.64 | |
| | Sigma Aldrich Fine Chemicals Biosciences Boc-Dap-OH >=98.0% (TLC) | 73259-81-1 | MFCD00236843 | 1G | Sigma Aldrich Fine Chemicals Biosciences | ₹ 9,380.80 | |
 | Boc-L-Dap-OH | ChemScene | ₹ 427.80 - ₹ 87,185.64 |
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Description
- Application: Reactant for:Protein assembly directed by synthetic molecular recognition motifsSolid phase synthesis of gramicidin S cyclic analogs with antibiotic and hemolytic activitiesSynthesis of HCV protease inhibitor modified analogsSolid phase synthesis of peptidic V1a receptor agonistsDirected peptide assembly at lipid-water interface
- Other Notes: Monoprotected derivative of DAP; used e.g. in the synthesis of glucosamine synthase inhibitors,[1][2] a myosin kinase inhibitor.[3] Preparation of peptides with metal complexing groups.[4]
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Quality Level: 100
Assay: ≥98.0% (TLC)
form: solid
optical activity: [α]20/D +5.5±1°, c = 1% in methanol: water (1:1)
reaction suitability: reaction type: Boc solid-phase peptide synthesis
impurities: ~3% water
mp: 210 °C (dec.)
application(s): peptide synthesis
SMILES string: CC(C)(C)OC(=O)N[C@@H](CN)C(O)=O
InChI: 1S/C8H16N2O4/c1-8(2,3)14-7(13)10-5(4-9)6(11)12/h5H,4,9H2,1-3H3,(H,10,13)(H,11,12)/t5-/m0/s1
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