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Merck
CN

15461

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
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
57647441
EC Number:
223-341-9
Beilstein/REAXYS Number:
4238574
MDL number:
MFCD00042760

Key Documents

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InChI key

PCZJWSPKNYONIM-VIFPVBQESA-N

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

SMILES string

CSCC[C@H](NC(=O)OC(C)(C)C)C(=O)ON1C(=O)CCC1=O

form

solid

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

Quality Level

100

Related Categories

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCBL5985V
1437588
421292/1
1191586
431950/1

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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
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

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