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20430

Sigma-Aldrich

Boc-OSu

≥98.0% (CHN), for peptide synthesis

Synonym(s):

N-(tert-Butoxycarbonyloxy)succinimide, tert-Butyl N-succinimidyl carbonate

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About This Item

Empirical Formula (Hill Notation):
C9H13NO5
CAS Number:
Molecular Weight:
215.20
Beilstein:
1536756
EC Number:
MDL number:
UNSPSC Code:
12352005
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22

product name

Boc-OSu, ≥98.0% (CHN)

Assay

≥98.0% (CHN)

form

solid

mp

~95 °C (dec.)

application(s)

peptide synthesis

storage temp.

−20°C

SMILES string

CC(C)(C)OC(=O)ON1C(=O)CCC1=O

InChI

1S/C9H13NO5/c1-9(2,3)14-8(13)15-10-6(11)4-5-7(10)12/h4-5H2,1-3H3

InChI key

VTGFSVGZCYYHLO-UHFFFAOYSA-N

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Other Notes

Boc-protecting group reagent

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

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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Stabilization of Bacillus subtilis -amylase by amino group acylation.
J Hora
Biochimica et biophysica acta, 310(1), 264-267 (1973-05-17)
H. Gross et al.
Justus Liebigs Annalen der Chemie, 725, 212-212 (1969)
M. Franke et al.
Tetrahedron Letters, 4765-4765 (1966)

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