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15461

Sigma-Aldrich

Boc-Met-OSu

Synonym(s):

Boc-L-methionine hydroxysuccinimide ester

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About This Item

Empirical Formula (Hill Notation):
C14H22N2O6S
CAS Number:
3845-64-5
Molecular Weight:
346.40
Beilstein:
4238574
EC Number:
223-341-9
MDL number:
MFCD00042760
UNSPSC Code:
12352209
PubChem Substance ID:
57647441
NACRES:
NA.22

form

solid

Quality Level

100

optical activity

[α]20/D −21.5±2°, c = 2% in dioxane

reaction suitability

reaction type: Boc solid-phase peptide synthesis

ign. residue

≤0.05%

mp

120-128 °C

application(s)

peptide synthesis

storage temp.

−20°C

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

PCZJWSPKNYONIM-VIFPVBQESA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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C W Basse et al.
The Journal of biological chemistry, 268(20), 14724-14731 (1993-07-15)
We have previously isolated glycopeptides derived from yeast invertase that acted as highly potent elicitors in suspension-cultured tomato cells, inducing ethylene biosynthesis and phenylalanine ammonia-lyase activity, and we have found that the high mannose oligosaccharides released from the pure glycopeptide
F Z Sheabar et al.
Chemical research in toxicology, 7(5), 650-658 (1994-09-01)
We report the chemical foundation for a new method to detect carcinogen-DNA adducts, which we have designated adduct detection by acylation with methionine (ADAM). The method is based on reaction of DNA adducts with a protected methionine derivative, (tert-butoxycarbonyl)-L-methionine N-hydroxysuccinimidyl

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