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Suberic acid

Suberic acid Structure
CAS No.
505-48-6
Chemical Name:
Suberic acid
Synonyms
OCTANEDIOIC ACID;suberic;octandioic acid;KORK ACID;CORK ACID;1,8-Octanedioic acid;142-144℃;Suberic aci;SUBERIC ACID;Undecanediol
CBNumber:
CB2775043
Molecular Formula:
C8H14O4
Molecular Weight:
174.19
MOL File:
505-48-6.mol
MSDS File:
SDS
Modify Date:
2025/1/27 9:38:02

Suberic acid Properties

Melting point 140-144 °C(lit.)
Boiling point 230 °C15 mm Hg(lit.)
Density 1.3010 (rough estimate)
bulk density 700kg/m3
vapor pressure 0Pa at 22.85℃
refractive index 1.4370 (estimate)
Flash point 203 °C
storage temp. Store below +30°C.
solubility 1.6g/l
form Powder
pka 4.52(at 25℃)
color White to cream
PH 3.79(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
Stability Stable. Combustible. Incompatible with strong oxidizing agents, reducing agents, bases.
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 Octanedioic acid (505-48-6)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P305+P351+P338
Hazard Codes  Xi
Risk Statements  36-36/37/38
Safety Statements  26-39-36
WGK Germany  1
Autoignition Temperature 430°C
TSCA  Yes
HS Code  29171990
NFPA 704
0
2 0

Suberic acid price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) S5200 Suberic acid 98% 505-48-6 5G ₹1374.78 2022-06-14 Buy
Sigma-Aldrich(India) S5200 Suberic acid 98% 505-48-6 100G ₹2803.68 2022-06-14 Buy
Sigma-Aldrich(India) S5200 Suberic acid 98% 505-48-6 500G ₹7718.23 2022-06-14 Buy
Sigma-Aldrich(India) 60930 Suberic acid purum, ≥98.0% (T) 505-48-6 100G ₹10121.38 2022-06-14 Buy
Sigma-Aldrich(India) 60930 Suberic acid purum, ≥98.0% (T) 505-48-6 250G ₹13769.4 2022-06-14 Buy
Product number Packaging Price Buy
S5200 5G ₹1374.78 Buy
S5200 100G ₹2803.68 Buy
S5200 500G ₹7718.23 Buy
60930 100G ₹10121.38 Buy
60930 250G ₹13769.4 Buy

Suberic acid Chemical Properties,Uses,Production

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

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

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 DEG 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.]

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Subericacid,99% 142-144℃ STRYCHNINE (P) Hexane-1,6-dicarboxylic acid, Suberic acid Cork Acid 1,6-Hexanedicarboxylic Acid Kork Acid Octanedioic Acid Suberic aci 1.6-Hexanedica Suberic acid purum, >=98.0% (T) Octanedioic acid for synthesis RARECHEM AL BO 0184 HEXANE-1,6-DICARBOXYLIC ACID DICARBOXYLIC ACID C8 1,6-Dicarboxyhexane 1,8-octanedioicacid Hexamethylenedicarboxylic acid Octane-1,8-dioic acid subericacid(octanedioicacid) 1,6-HEXANEDICARBOXYLIC ACID Oktanedioic acid SUBERIC ACID OCTANEDIOC ACID SubericAcid> suberate (octanedioate) KORK ACID octandioic acid CORK ACID 1,8-Octanedioic acid suberic OCTANEDIOIC ACID Undecanediol Suberic Acid/ 1,6-Hexanedicarboxylic Acid / Octanedioic Acid. Octanedioic acid|||1,8-Octanedioic acid Suberic Acid (Impurity B) Repaglinide Impurity 21 Suberic acid, 10 mM in DMSO Suberic acid, 98% 505-48-6 CH26COOH2 HOOCCH26COOH HO2CCH26CO2H Organic Building Blocks Building Blocks C8 Carbonyl Compounds Carboxylic Acids 伪,蠅-Alkanedicarboxylic Acids Monofunctional & 伪,蠅-Bifunctional Alkanes 伪,蠅-Bifunctional Alkanes Pharmaceutical intermediates Dicarboxylic Acids Biochemicals and Reagents Building Blocks C8 Carbonyl Compounds Carboxylic Acids Chemical Synthesis Fatty Acids and conjugates Fatty Acyls