408484
Boc-Arg-OH
for peptide synthesis
Manufacturer: Sigma Aldrich
CAS Number: 13726-76-6
Synonym(S): Nα-(tert-Butoxycarbonyl)-L-arginine, Nα-Boc-L-arginine
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 G | 408484-5-G | In Stock | ₹ 15,566.35 |
408484 - 5 G
In Stock
Quantity
1
Base Price: ₹ 15,566.35
GST (18%): ₹ 2,801.943
Total Price: ₹ 18,368.293
product name
Boc-Arg-OH,
form
powder
Quality Level
100
optical activity
[α]20/D −6.5°, c = 1 in acetic acid
reaction suitability
reaction type: Boc solid-phase peptide synthesis
impurities
5-10% n-butanol
application(s)
peptide synthesis
SMILES string
CC(C)(C)OC(=O)N[C@@H](CCCNC(N)=N)C(O)=O
InChI
1S/C11H22N4O4/c1-11(2,3)19-10(18)15-7(8(16)17)5-4-6-14-9(12)13/h7H,4-6H2,1-3H3,(H,15,18)(H,16,17)(H4,12,13,14)/t7-/m0/s1
InChI key
HSQIYOPBCOPMSS-ZETCQYMHSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | (S)-2-((tert-Butoxycarbonyl)amino)-5-guanidinopentanoic acid | ChemScene | ₹ 598.92 - ₹ 18,823.20 |
Related Products
Description
- Application: Studying the kinetics of tanning reactions: The study compares the color development kinetics in tanning reactions involving dihydroxyacetone with both free and Boc-protected basic amino acids, highlighting Boc-Arg-OH′s role in stabilizing reactive intermediates in cosmetic chemistry (Sun et al., 2022).Protonation states in peptide synthesis: This research examines the side-chain protonation states of a fluorescent arginine derivative, including Boc-Arg-OH, to optimize fluorescence in peptide synthesis for bioimaging applications (Marshall et al., 2019).
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
235.4 °F
Flash Point(C)
113 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
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product name: Boc-Arg-OH,
form: powder
Quality Level: 100
optical activity: [α]20/D −6.5°, c = 1 in acetic acid
reaction suitability: reaction type: Boc solid-phase peptide synthesis
impurities: 5-10% n-butanol
application(s): peptide synthesis
SMILES string: CC(C)(C)OC(=O)N[C@@H](CCCNC(N)=N)C(O)=O
InChI: 1S/C11H22N4O4/c1-11(2,3)19-10(18)15-7(8(16)17)5-4-6-14-9(12)13/h7H,4-6H2,1-3H3,(H,15,18)(H,16,17)(H4,12,13,14)/t7-/m0/s1
InChI key: HSQIYOPBCOPMSS-ZETCQYMHSA-N
product name:
Boc-Arg-OH,
form:
powder
Quality Level:
100
optical activity:
[α]20/D −6.5°, c = 1 in acetic acid
reaction suitability:
reaction type: Boc solid-phase peptide synthesis
impurities:
5-10% n-butanol
application(s):
peptide synthesis
SMILES string:
CC(C)(C)OC(=O)N[C@@H](CCCNC(N)=N)C(O)=O
InChI:
1S/C11H22N4O4/c1-11(2,3)19-10(18)15-7(8(16)17)5-4-6-14-9(12)13/h7H,4-6H2,1-3H3,(H,15,18)(H,16,17)(H4,12,13,14)/t7-/m0/s1
InChI key:
HSQIYOPBCOPMSS-ZETCQYMHSA-N
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