![N,3,3-trimethylbicyclo[2.2.1]heptan-2-amine hydrochloride AldrichCPR](/deepweb/assets/sigmaaldrich/product/structures/302/422/dae3439e-735d-4d67-8652-5997279d7417/640/dae3439e-735d-4d67-8652-5997279d7417.png)
Yes. The 3D structure of Product 33240 is not determined and it is a mixture of various structural patterns.
33240
2,6-Diaminopimelic acid
≥95.0% (NT), for peptide synthesis
Synonym(s):
2,6-Diaminoheptanedioic acid
Sign Into View Organizational & Contract Pricing
Select a Size
1 G
€57.90
5 G
€179.00
All Photos(1)
Select a Size
Change View
1 G
€57.90
5 G
€179.00
About This Item
Linear Formula:
HOOCCH(NH2)(CH2)3CH(NH2)COOH
CAS Number:
Molecular Weight:
190.20
Beilstein:
1787719
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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
Looking for similar products? Visit Product Comparison Guide
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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)
Peter Kämpfer et al.
International journal of systematic and evolutionary microbiology, 64(Pt 5), 1811-1816 (2014-02-22)
A Gram-staining-positive, aerobic, non-endospore forming organism, isolated as a seed endophyte (colonizing the internal healthy tissue of plant seed) of sweet corn (Zea mays), strain CSE-5610T, was studied for its taxonomic allocation. On the basis of 16S rRNA gene sequence
Sarah N Buss et al.
International journal of systematic and evolutionary microbiology, 63(Pt 11), 4087-4093 (2013-06-04)
A Gram-staining-positive, endospore-forming rod was isolated independently from clinical specimens in New York State, USA, once in 2009 and twice in 2011. The three isolates had identical 16S rRNA gene sequences and, based on their 16S rRNA gene sequence, are
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)
Lilian Hor et al.
Biochimie, 95(10), 1949-1953 (2013-07-11)
DAP epimerase is the penultimate enzyme in the lysine biosynthesis pathway. The most versatile assay for DAP epimerase catalytic activity employs a coupled DAP epimerase-DAP dehydrogenase enzyme system with a commercial mixture of DAP isomers as substrate. DAP dehydrogenase converts
-
商品番号33240の”2,6-ジアミノピメリン酸”の、立体構造に関して質問があります。 こちらアミノ基の立体構造が明記されておりませんが、商品番号92951のように立体構造が決定されておらず、様々な構造のパターンが混合しているという認識でよろしいでしょうか。ご回答宜しくお願いします。
1 answer-
Helpful?
-
-
Hello, How to dissolve 2,6 diamino pimelic acid? And what is the maximum conetration?
1 answer-
2,6-Diaminopimelic acid is a highly polar molecule, soluble in water or dilute acidic/basic solutions. It also has documented solubility in polar organic solvents such as methanol and DMSO. A documented maximum concentration is not available and would need to be determined experimentally for the chosen solvent/temperature.
Helpful?
-
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
