Home Other Building Blocks N-(2-Carboxyethyl)-N-dodecyl-beta-alanine

N-(2-Carboxyethyl)-N-dodecyl-beta-alanine

CAS No.:
17066-08-9
Catalog Number:
AG003ADW
Molecular Formula:
C18H35NO4
Molecular Weight:
329.4748
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Product Description
Catalog Number:
AG003ADW
Chemical Name:
N-(2-Carboxyethyl)-N-dodecyl-beta-alanine
CAS Number:
17066-08-9
Molecular Formula:
C18H35NO4
Molecular Weight:
329.4748
IUPAC Name:
3-[2-carboxyethyl(dodecyl)amino]propanoic acid
InChI:
InChI=1S/C18H35NO4/c1-2-3-4-5-6-7-8-9-10-11-14-19(15-12-17(20)21)16-13-18(22)23/h2-16H2,1H3,(H,20,21)(H,22,23)
InChI Key:
XYYUAOIALFMRGY-UHFFFAOYSA-N
SMILES:
CCCCCCCCCCCCN(CCC(=O)O)CCC(=O)O
EC Number:
241-127-3
UNII:
G6L51RHM7E
Properties
Complexity:
289  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
329.257g/mol
Formal Charge:
0
Heavy Atom Count:
23  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
329.481g/mol
Monoisotopic Mass:
329.257g/mol
Rotatable Bond Count:
17  
Topological Polar Surface Area:
77.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.6  
Literature
Title Journal
Temperature dependence of electron transfer to the M-side bacteriopheophytin in rhodobacter capsulatus reaction centers. The journal of physical chemistry. B 20080501
Deriphat 2-DE to visualize polyphenol oxidase in Moscato and Prosecco grapes. Electrophoresis 20071101
B-side charge separation in bacterial photosynthetic reaction centers: nanosecond time scale electron transfer from HB- to QB. Biochemistry 20030225
Quinone reduction via secondary B-branch electron transfer in mutant bacterial reaction centers. Biochemistry 20030218
Properties