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408468

Sigma-Aldrich

Boc-Asp-OH

99%

Synonym(s):

N-(tert-Butoxycarbonyl)-L-aspartic acid, Boc-L-aspartic acid

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About This Item

Linear Formula:
(CH3)3COCONHCH(COOH)CH2COOH
CAS Number:
13726-67-5
Molecular Weight:
233.22
Beilstein/REAXYS Number:
1913973
EC Number:
237-294-7
MDL number:
MFCD00037279
UNSPSC Code:
12352209
PubChem Substance ID:
24865571
NACRES:
NA.22

assay

99%

form

solid

optical activity

[α]20/D −6.0°, c = 1 in methanol

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

116-118 °C (lit.)

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N[C@@H](CC(O)=O)C(O)=O

InChI

1S/C9H15NO6/c1-9(2,3)16-8(15)10-5(7(13)14)4-6(11)12/h5H,4H2,1-3H3,(H,10,15)(H,11,12)(H,13,14)/t5-/m0/s1

InChI key

KAJBMCZQVSQJDE-YFKPBYRVSA-N

Gene Information

human ... CA1(759) , CA2(760)

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
09919TE
00527ME
15622CU
09706EF
07112PR

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Acta biomaterialia, 10(11), 4583-4596 (2014-07-23)
Nanoparticles (NP) that target bone tissue were developed using PLGA-PEG (poly(lactic-co-glycolic acid)-polyethylene glycol) diblock copolymers and bone-targeting moieties based on aspartic acid, (Asp)(n(1,3)). These NP are expected to enable the transport of hydrophobic drugs. The molecular structures were examined by

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