33240
2,6-Diaminopimelic acid
≥95.0% (NT), for peptide synthesis
Synonym(s):
2,6-Diaminoheptanedioic acid
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About This Item
Linear Formula:
HOOCCH(NH2)(CH2)3CH(NH2)COOH
CAS Number:
Molecular Weight:
190.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
EC Number:
209-524-6
MDL number:
Beilstein/REAXYS Number:
1787719
Product Name
2,6-Diaminopimelic acid, ≥95.0% (NT)
Quality Level
assay
≥95.0% (NT)
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
mp
~295 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
NC(CCCC(N)C(O)=O)C(O)=O
InChI
1S/C7H14N2O4/c8-4(6(10)11)2-1-3-5(9)7(12)13/h4-5H,1-3,8-9H2,(H,10,11)(H,12,13)
InChI key
GMKMEZVLHJARHF-UHFFFAOYSA-N
Application
2,6-Diaminopimelic acid (2,6-DAP) can be used as a building block in the synthesis of tripeptides , and γ-glutamyldiaminopimelic acid derivatives.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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A new stereocontrolled synthesis of uncommon tripeptides derived from 2, 6-diaminopimelic acid (2, 6-DAP)
Paradisi F, et al.
Tetrahedron Asymmetry, 12(23), 3319-3324 (2001)
Structure- activity relationships in nucleotide oligomerization domain 1 (Nod1) agonistic γ-glutamyldiaminopimelic acid derivatives
Agnihotri G, et al.
Journal of Medicinal Chemistry, 54(5), 1490-1510 (2011)
Geun-Hye Lee et al.
International journal of systematic and evolutionary microbiology, 64(Pt 5), 1622-1628 (2014-02-04)
Two novel bacterial strains, GH2-4T and GH2-5, were isolated from mangrove soil near the seashore of Weno island in Chuuk state, Micronesia, and were characterized by a polyphasic approach. The two strains were strictly aerobic, Gram-staining-positive, motile, endospore-forming rods that