855294
8-Aminooctanoic acid
99%
Synonym(s):
ω-Aminocaprylic acid
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About This Item
Linear Formula:
NH2(CH2)7COOH
CAS Number:
Molecular Weight:
159.23
Beilstein:
1756493
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
mp
194 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
NCCCCCCCC(O)=O
InChI
1S/C8H17NO2/c9-7-5-3-1-2-4-6-8(10)11/h1-7,9H2,(H,10,11)
InChI key
UQXNEWQGGVUVQA-UHFFFAOYSA-N
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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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A J Dobson et al.
Acta crystallographica. Section C, Crystal structure communications, 54 ( Pt 7), 969-972 (1998-09-18)
The title acid, 8-aminooctanoic acid, C8H17NO2, crystallized in the centrosymmetric space group P2(1)/n in the zwitterionic form. The three H atoms involved in hydrogen bonding are ordered. The five intermolecular N-H...O hydrogen bonds have N...O distances ranging from 2.752 (2)
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E J Demant
Biochimica et biophysica acta, 1304(1), 43-55 (1996-11-11)
Using a hydrophobic 8-aminooctanoic acid cross-linker, the pH-indicator dye 7-hydroxycoumarin-4-acetic acid (7-HCA) is covalently bound to bovine serum albumin (BSA) at the positions of reactive amino groups. A highly stable and water-soluble complex (BSA-HCA) with a 1:4 molar stoichiometry is
T P Hicks et al.
Neuroscience letters, 57(3), 295-299 (1985-06-24)
The 8-carbon chain analogue of gamma-aminobutyric acid (GABA), omega-aminocaprylic acid (omega-AC), was administered to single cortical neurones of rat by microiontophoresis and its effect on cell firing compared to the effect elicited by GABA. The spontaneous and glutamate-elicited firing rates
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