60930
Suberic acid
purum, ≥98.0% (T)
Synonym(s):
Octanedioic acid
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About This Item
Linear Formula:
HOOC(CH2)6COOH
CAS Number:
Molecular Weight:
174.19
Beilstein:
1210161
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
purum
Quality Level
Assay
≥98.0% (T)
bp
230 °C/15 mmHg (lit.)
mp
140-144 °C (lit.)
140-144 °C
SMILES string
OC(=O)CCCCCCC(O)=O
InChI
1S/C8H14O4/c9-7(10)5-3-1-2-4-6-8(11)12/h1-6H2,(H,9,10)(H,11,12)
InChI key
TYFQFVWCELRYAO-UHFFFAOYSA-N
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Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
410.0 °F - closed cup
Flash Point(C)
210 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
Taishi Yokoi et al.
Dalton transactions (Cambridge, England : 2003), 41(9), 2732-2737 (2012-01-18)
Octacalcium phosphates (OCPs) co-incorporated with various molar ratios of succinate and suberate ions were synthesized by wet processing. The interplanar spacings of the (100) planes (d(100)) of OCPs formed in the presence of succinic acid (Suc) or suberic acid (Sub)
Ronald J Nachman et al.
Peptides, 26(1), 115-120 (2005-01-01)
The aliphatic amino diacid alpha-aminosuberic acid can function as an effective, stable mimic of the hydrolysis-susceptible Tyr(SO3H) group in sulfakinin neuropeptide analogs for both hindgut contractile activity in cockroach and food intake-inhibition activity in the desert locust. In the analog
M Rivard et al.
Amino acids, 15(4), 389-392 (1999-01-19)
Papain-catalyzed regioselective cleavage of alpha-methyl ester in Z-DL-Asu(OMe)-OMe leads to Z-L-Asu(OMe)-OH and Z-D-Asu(OMe)-OMe. Subsequent saponifications yield Z-L-Asu-OH and Z-D-Asu-OH. The enzymatic alpha-ester hydrolysis was also achieved by subtilisin BPN' in organic solvent with low water content.
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
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