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Merck
모든 사진(1)

문서

60930

Sigma-Aldrich

Suberic acid

purum, ≥98.0% (T)

동의어(들):

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 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

purum

Quality Level

분석

≥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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픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

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

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

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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