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About This Item
Linear Formula:
HOOC(CH2)6COOH
CAS Number:
Molecular Weight:
174.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-010-9
Beilstein/REAXYS Number:
1210161
MDL number:
Assay:
≥98.0% (T)
InChI key
TYFQFVWCELRYAO-UHFFFAOYSA-N
InChI
1S/C8H14O4/c9-7(10)5-3-1-2-4-6-8(11)12/h1-6H2,(H,9,10)(H,11,12)
SMILES string
OC(=O)CCCCCCC(O)=O
grade
purum
assay
≥98.0% (T)
bp
230 °C/15 mmHg (lit.)
Quality Level
functional group
carboxylic acid
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
410.0 °F - closed cup
flash_point_c
210 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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S Hayakawa
Zeitschrift fur allgemeine Mikrobiologie, 22(5), 309-326 (1982-01-01)
Through the isolation and identification of a wide variety of degradation products formed from bile acids by microorganisms, a unified scheme for the complete degradation of bile acids to carbon dioxide and water has been proposed and discussed. The proposed
Xu Dong Zhang et al.
Biochemical pharmacology, 66(8), 1537-1545 (2003-10-14)
TRAIL appears to be a promising anticancer agent in that it induces apoptosis in a wide range of cancer cells but not normal tissues. Sensitivity of melanoma cells to TRAIL-induced apoptosis varied considerably because of their development of various resistance
R J Truscott et al.
Clinica chimica acta; international journal of clinical chemistry, 94(1), 31-39 (1979-05-16)
The urine of a child who presented with an episode of a disease resembling Reye's syndrome was found to contain large quantities of the dicarboxylic acids adipic and suberic acids, as well as the glycine conjugate of suberic acid, suberyl
Q Gao et al.
Acta crystallographica. Section B, Structural science, 50 ( Pt 6), 695-703 (1994-12-01)
Neutron diffraction data for suberic acid [HOOC(CH2)6COOH] were collected at 18.4, 75 and 123 K using a twinned crystal. The neutron data reduction included derivation of a complete set of corrected intensities, as if from a single crystal. This was
Monica Ilies et al.
Bioorganic & medicinal chemistry, 11(10), 2227-2239 (2003-04-26)
Novel matrix metalloproteinase (MMP)/bacterial collagenase inhibitors are reported, considering the sulfonylated amino acid hydroxamates as lead molecules. A series of compounds was prepared by reaction of arylsulfonyl isocyanates with N-(5H-dibenzo[a,d]cyclohepten-5-yl)- and N-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl) methyl glycocolate, respectively, followed by the conversion of
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