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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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC8675
BCBS3067V
BCBK0414V
BCBC3867V
BCBC3867

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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
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

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