Identification | More | [Name]
Suberic acid | [CAS]
505-48-6 | [Synonyms]
1,6-HEXANEDICARBOXYLIC ACID CORK ACID DICARBOXYLIC ACID C8 HEXANE-1,6-DICARBOXYLIC ACID KORK ACID OCTANEDIOC ACID OCTANEDIOIC ACID RARECHEM AL BO 0184 SUBERIC ACID 1,6-Dicarboxyhexane 1,8-Octanedioic acid 1,8-octanedioicacid Hexamethylenedicarboxylic acid Octane-1,8-dioic acid suberic subericacid(octanedioicacid) Oktanedioic acid Subericacid,99% 142-144℃ octandioic acid | [EINECS(EC#)]
208-010-9 | [Molecular Formula]
C8H14O4 | [MDL Number]
MFCD00004428 | [Molecular Weight]
174.19 | [MOL File]
505-48-6.mol |
Chemical Properties | Back Directory | [Appearance]
off-white crystalline powder | [Melting point ]
140-144 °C(lit.)
| [Boiling point ]
230 °C15 mm Hg(lit.)
| [density ]
1.3010 (rough estimate) | [vapor pressure ]
0Pa at 22.85℃ | [refractive index ]
1.4370 (estimate) | [Fp ]
203 °C
| [storage temp. ]
Store below +30°C. | [solubility ]
1.6g/l | [form ]
Powder | [pka]
4.52(at 25℃) | [color ]
White to cream | [PH]
3.2 (1.6g/l, H2O, 20℃) | [Stability:]
Stable. Combustible. Incompatible with strong oxidizing agents, reducing agents, bases. | [Water Solubility ]
0.6 g/L (20 ºC) | [Merck ]
14,8862 | [BRN ]
1210161 | [InChIKey]
TYFQFVWCELRYAO-UHFFFAOYSA-N | [LogP]
0.59 at 25℃ and pH7.08 | [CAS DataBase Reference]
505-48-6(CAS DataBase Reference) | [NIST Chemistry Reference]
Octanedioic acid(505-48-6) | [EPA Substance Registry System]
505-48-6(EPA Substance) |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36:Irritating to the eyes. R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S39:Wear eye/face protection . S36:Wear suitable protective clothing . | [WGK Germany ]
1
| [TSCA ]
Yes | [HS Code ]
29171990 |
Hazard Information | Back Directory | [Description]
It was firstly produced by nitric acid oxidation of cork (Latin suber) material and then from castor oil. The oxidation of ricinoleic acid produces, by splitting at the level of the double bond and at the level of the OH group, at the same time, suberic acid (octanedioic acid) and the next homologue azelaic acid. Suberic acid was used in the manufacture of alkyd resins and in the synthesis of polyamides leading to nylon. | [Chemical Properties]
off-white crystalline powder | [Uses]
In the plastics industry. | [Uses]
Suberic Acid is used in the preparation of reduction-sensitive micelles affecting their cellular uptake. This has potential application in delivery of anticancer drugs. It is also used in the fluoresc
ent detection of amidinium-carboxylate and amidinium formation. | [Definition]
ChEBI: An alpha,omega-dicarboxylic acid that is the 1,6-dicarboxy derivative of hexane. | [Synthesis Reference(s)]
Journal of the American Chemical Society, 81, p. 3677, 1959 DOI: 10.1021/ja01523a046 | [storage]
Store at -20°C | [Purification Methods]
Crystallise it from acetone. It sublimes at 300o without decomposition. [Beilstein 2 IV 2028.] |
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