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Key Documents

15052

Sigma-Aldrich

Boc-Ala-ONp

≥96.0% (HPLC)

Synonym(s):

Boc-L-alanine 4-nitrophenyl ester

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About This Item

Empirical Formula (Hill Notation):
C14H18N2O6
CAS Number:
2483-49-0
Molecular Weight:
310.30
Beilstein:
1892073
EC Number:
219-621-5
MDL number:
MFCD00038117
UNSPSC Code:
12352202
PubChem Substance ID:
57647282
NACRES:
NA.22

Quality Level

100

Assay

≥96.0% (HPLC)

reaction suitability

reaction type: Boc solid-phase peptide synthesis

application(s)

peptide synthesis

storage temp.

2-8°C

SMILES string

C[C@H](NC(=O)OC(C)(C)C)C(=O)Oc1ccc(cc1)[N+]([O-])=O

InChI

1S/C14H18N2O6/c1-9(15-13(18)22-14(2,3)4)12(17)21-11-7-5-10(6-8-11)16(19)20/h5-9H,1-4H3,(H,15,18)/t9-/m0/s1

InChI key

SUHFNHHZORGDFI-VIFPVBQESA-N

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Related Categories

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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J L Sohl et al.
Biochemistry, 36(13), 3894-3902 (1997-04-01)
alpha-Lytic protease, a chymotrypsin-like serine protease, is synthesized with an N-terminal 166 amino acid pro region which is absolutely required for folding of the protease. The pro region is also the most potent inhibitor of the protease known with a
H M Korchak et al.
The Journal of biological chemistry, 259(12), 7439-7445 (1984-06-25)
Activated neutrophils aggregate, generate superoxide (O-2), and degranulate. The role of Ca as "second messenger" in neutrophil activation was examined using as agonist the chemotactic peptide fMet-Leu-Phe and its antagonist t-butoxycarbonyl-Phe-Leu-Phe-Leu-Phe to systematically vary the time of receptor occupancy. Release

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