- Suberic acid
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- $29.00 / 1g
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2026-04-22
- CAS:505-48-6
- Min. Order:
- Purity: 99.80%
- Supply Ability: 10g
- Suberic acid
-
- $1.00 / 1kg
-
2026-03-20
- CAS:505-48-6
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 10 mt
- Suberic acid
-
- $0.00 / 1KG
-
2022-02-19
- CAS:505-48-6
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 100 tons
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| | Suberic acid Basic information |
| | Suberic acid Chemical Properties |
| Melting point | 140-144 °C(lit.) | | Boiling point | 230 °C15 mm Hg(lit.) | | bulk density | 700kg/m3 | | 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 | | pka | 4.52(at 25℃) | | form | Powder | | color | White to cream | | PH | 3.79(1 mM solution);3.27(10 mM solution);2.76(100 mM solution); | | Water Solubility | 0.6 g/L (20 ºC) | | Merck | 14,8862 | | BRN | 1210161 | | Henry's Law Constant | 1.8×106 mol/(m3Pa) at 25℃, Duchowicz et al. (2020) | | Stability: | Stable. Combustible. Incompatible with strong oxidizing agents, reducing agents, bases. | | InChI | 1S/C8H14O4/c9-7(10)5-3-1-2-4-6-8(11)12/h1-6H2,(H,9,10)(H,11,12) | | InChIKey | TYFQFVWCELRYAO-UHFFFAOYSA-N | | SMILES | OC(=O)CCCCCCC(O)=O | | 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 | Octanedioic acid (505-48-6) |
| Hazard Codes | Xi | | Risk Statements | 36-36/37/38 | | Safety Statements | 26-39-36 | | WGK Germany | 1 | | Autoignition Temperature | 430°C | | TSCA | TSCA listed | | HS Code | 29171990 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2 |
| | Suberic acid Usage And Synthesis |
| 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 fluorescent detection of amidinium-carboxylate and amidinium formation. | | Definition | ChEBI: An alpha,omega-dicarboxylic acid that is the 1,6-dicarboxy derivative of hexane. | | Reactions | Suberic acid is an essential chemical widespread in softwood trees' trunk. Can there be reactions such as esterification, carboxylic acid halides, amidation and reduction in suberic acid, generation pyrolysis is heated. Its main application is to react with dibasic alcohol and diamine, produce polyester and polymeric amide, and also for organic synthesis.
| | Synthesis Reference(s) | Journal of the American Chemical Society, 81, p. 3677, 1959 DOI: 10.1021/ja01523a046 | | Synthesis | Industrial is to be obtained by Viscotrol C or ricinolic acid or cyclooctane oxidation, conventionally using 50% sulfuric acid to carry out catalysis. Suberic acid also can be oxidized and obtained by cyclooctene. A method for preparing suberic acid through cyclooctene oxidation comprises the following steps: mixing tetra-allkylammonium perrhenate and alkyl-imidazolim disulfate ionic liquid in a certain proportion to form a composite phase transfer catalyst and meanwhile carrying out catalytic oxidation reaction on cyclooctene in the presence of alkyl-imidazolim disulfate ionic liquid serving as a reaction solvent and a hydrogen peroxide solution serving as an oxidizing agent, wherein the reaction temperature is 40-70°C, the pressure is normal, and the reaction time is 0.5-4 hours. After the reaction, the gas chromatography detection shows that the conversion rate of the cyclooctene is above 90%, and the cyclooctene yield is above 60%.
| | Purification Methods | Crystallise it from acetone. It sublimes at 300o without decomposition. [Beilstein 2 IV 2028.] | | Toxics Screening Level | The initial threshold screening level (ITSL) for suberic acid is 17 μg/m3 based on an annual averaging time. |
| | Suberic acid Preparation Products And Raw materials |
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