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Sigma-Aldrich

L-Aspartic acid dimethyl ester hydrochloride

97%

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Synonym(s):
Dimethyl L-aspartate hydrochloride, L-Asp(OMe)OMe·HCl
Linear Formula:
CH3O2CCH2CH(NH2)CO2CH3 · HCl
CAS Number:
32213-95-9
Molecular Weight:
197.62
MDL number:
MFCD00038878
UNSPSC Code:
12352200
PubChem Substance ID:
24869140
NACRES:
NA.22

Assay

97%

form

solid

reaction suitability

reaction type: solution phase peptide synthesis

mp

115-117 °C (lit.)

application(s)

peptide synthesis

SMILES string

Cl.COC(=O)C[C@H](N)C(=O)OC

InChI

1S/C6H11NO4.ClH/c1-10-5(8)3-4(7)6(9)11-2;/h4H,3,7H2,1-2H3;1H/t4-;/m0./s1

InChI key

PNLXWGDXZOYUKB-WCCKRBBISA-N

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WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Pharmaceutics, 12(9) (2020-09-10)
An elevated level of endoplasmic reticulum (ER) stress is considered an aggravating factor for inflammatory bowel disease (IBD). To develop an ER-stress attenuator that is effective against colitis, 4-phenylbutyric acid (4-PBA), a chemical chaperone that alleviates ER stress, was conjugated
Wooseong Kim et al.
Molecular pharmaceutics, 16(9), 4007-4016 (2019-08-07)
We investigated if the therapeutic switching of sofalcone (SFC), a gastroprotective agent, to an anticolitic agent is feasible using colon-targeted drug delivery. SFC can activate the anti-inflammatory nuclear factor (erythroid-derived 2)-like 2 (Nrf2)-hemeoxygenase-1 (HO-1) pathway in human colon epithelial cells

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