Boc-Dap-OH

ALDRICH/15402 - ≥98.0% (TLC)

Synonym: (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; N_α-Boc-L-2,3-diaminopropionic acid; Boc-Dpr-OH

CAS Number: 73259-81-1
Empirical Formula (Hill Notation): C₈H₁₆N₂O₄
Molecular Weight: 204.22
MDL Number: MFCD00236843
Linear Formula: C₈H₁₆N₂O₄
Product Type: Chemical

Catalog Number	PKG Qty.	Price


45-15402-1G	1 g	$86.80 1/EA	Add To Favorites
45-15402-5G	5 g	$390.00 1/EA	Add To Favorites

Properties
Descriptions
Safety Info.
Basic Data

application(s)	peptide synthesis
assay	≥98.0% (TLC)
form	solid
impurities	~3% water
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
InChI key	KRJLRVZLNABMAT-YFKPBYRVSA-N
mp	210 °C (dec.)
optical activity	[α]20/D +5.5±1°, c = 1% in methanol: water (1:1)
Quality Level	100
reaction suitability	reaction type: Boc solid-phase peptide synthesis
SMILES string	CC(C)(C)OC(=O)N[C@@H](CN)C(O)=O

Application:	Reactant for: • Protein assembly directed by synthetic molecular recognition motifs • Solid phase synthesis of gramicidin S cyclic analogs with antibiotic and hemolytic activities • Synthesis of HCV protease inhibitor modified analogs • Solid phase synthesis of peptidic V1a receptor agonists • Directed peptide assembly at lipid-water interface
Other Notes:	Monoprotected derivative of DAP; used e.g. in the synthesis of glucosamine synthase inhibitors, a myosin kinase inhibitor. Preparation of peptides with metal complexing groups.
Packaging:	1, 5 g in glass bottle

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

Purity	≥98.0% (TLC)
mp	210 °C (dec.)
UNSPSC	12352200

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