15456
Boc-Lys-OH
≥99.0% (NT)
Manufacturer: Sigma Aldrich
CAS Number: 13734-28-6
Synonym(S): Nα-(tert-Butoxycarbonyl)-L-lysine, Nα-Boc-L-lysine
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 G | 15456-5-G | In Stock | ₹ 11,333.78 |
| 25 G | 15456-25-G | In Stock | ₹ 51,472.88 |
15456 - 5 G
In Stock
Quantity
1
Base Price: ₹ 11,333.78
GST (18%): ₹ 2,040.08
Total Price: ₹ 13,373.86
Quality Level
200
Assay
≥99.0% (NT)
form
solid
optical activity
[α]20/D +4.6±0.5°, c = 2% in H2O
reaction suitability
reaction type: Boc solid-phase peptide synthesis
mp
~205 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
CC(C)(C)OC(=O)N[C@@H](CCCCN)C(O)=O
InChI
1S/C11H22N2O4/c1-11(2,3)17-10(16)13-8(9(14)15)6-4-5-7-12/h8H,4-7,12H2,1-3H3,(H,13,16)(H,14,15)/t8-/m0/s1
InChI key
DQUHYEDEGRNAFO-QMMMGPOBSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Boc-Lys-OH | Sigma Aldrich | ₹ 6,278.50 | |
 | Boc-Lys-OH | ChemScene | ₹ 598.92 - ₹ 43,550.04 |
Related Products
Description
- General description: Boc-Lys-OH also known as Nα-Boc-L-lysine, is an amino acid derivative of lysine which is used in solid phase peptide synthesis.
- Application: Boc-Lys-OH is used as a building block to form peptides that have bioorthogonal reactive groups via boc protected solid phase synthesis. [1]
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
Compare Similar Items
Show Difference
Quality Level: 200
Assay: ≥99.0% (NT)
form: solid
optical activity: [α]20/D +4.6±0.5°, c = 2% in H2O
reaction suitability: reaction type: Boc solid-phase peptide synthesis
mp: ~205 °C (dec.) (lit.)
application(s): peptide synthesis
SMILES string: CC(C)(C)OC(=O)N[C@@H](CCCCN)C(O)=O
InChI: 1S/C11H22N2O4/c1-11(2,3)17-10(16)13-8(9(14)15)6-4-5-7-12/h8H,4-7,12H2,1-3H3,(H,13,16)(H,14,15)/t8-/m0/s1
InChI key: DQUHYEDEGRNAFO-QMMMGPOBSA-N
Quality Level:
200
Assay:
≥99.0% (NT)
form:
solid
optical activity:
[α]20/D +4.6±0.5°, c = 2% in H2O
reaction suitability:
reaction type: Boc solid-phase peptide synthesis
mp:
~205 °C (dec.) (lit.)
application(s):
peptide synthesis
SMILES string:
CC(C)(C)OC(=O)N[C@@H](CCCCN)C(O)=O
InChI:
1S/C11H22N2O4/c1-11(2,3)17-10(16)13-8(9(14)15)6-4-5-7-12/h8H,4-7,12H2,1-3H3,(H,13,16)(H,14,15)/t8-/m0/s1
InChI key:
DQUHYEDEGRNAFO-QMMMGPOBSA-N
Quality Level: 200
Assay: ≥98%
form: liquid
optical activity: __
reaction suitability: __
mp: __
application(s): __
SMILES string: COc1cccc2ccccc12
InChI: 1S/C11H10O/c1-12-11-8-4-6-9-5-2-3-7-10(9)11/h2-8H,1H3
InChI key: NQMUGNMMFTYOHK-UHFFFAOYSA-N
Quality Level:
200
Assay:
≥98%
form:
liquid
optical activity:
__
reaction suitability:
__
mp:
__
application(s):
__
SMILES string:
COc1cccc2ccccc12
InChI:
1S/C11H10O/c1-12-11-8-4-6-9-5-2-3-7-10(9)11/h2-8H,1H3
InChI key:
NQMUGNMMFTYOHK-UHFFFAOYSA-N
Quality Level: __
Assay: __
form: __
optical activity: __
reaction suitability: __
mp: __
application(s): __
SMILES string: __
InChI: __
InChI key: __
Quality Level:
__
Assay:
__
form:
__
optical activity:
__
reaction suitability:
__
mp:
__
application(s):
__
SMILES string:
__
InChI:
__
InChI key:
__
Quality Level: 100
Assay: __
form: solid
optical activity: [α]20/D −21.5±2°, c = 2% in dioxane
reaction suitability: reaction type: Boc solid-phase peptide synthesis
mp: 120-128 °C
application(s): peptide synthesis
SMILES string: CSCC[C@H](NC(=O)OC(C)(C)C)C(=O)ON1C(=O)CCC1=O
InChI: 1S/C14H22N2O6S/c1-14(2,3)21-13(20)15-9(7-8-23-4)12(19)22-16-10(17)5-6-11(16)18/h9H,5-8H2,1-4H3,(H,15,20)/t9-/m0/s1
InChI key: __
Quality Level:
100
Assay:
__
form:
solid
optical activity:
[α]20/D −21.5±2°, c = 2% in dioxane
reaction suitability:
reaction type: Boc solid-phase peptide synthesis
mp:
120-128 °C
application(s):
peptide synthesis
SMILES string:
CSCC[C@H](NC(=O)OC(C)(C)C)C(=O)ON1C(=O)CCC1=O
InChI:
1S/C14H22N2O6S/c1-14(2,3)21-13(20)15-9(7-8-23-4)12(19)22-16-10(17)5-6-11(16)18/h9H,5-8H2,1-4H3,(H,15,20)/t9-/m0/s1
InChI key:
__