ChemicalBook > CAS DataBase List > Suberic acid

Suberic acid

Product Name
Suberic acid
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
Formula Weight
174.19
MOL File
505-48-6.mol
More
Less

Suberic acid Property

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)
More
Less

Safety

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
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H319Causes serious eye irritation

Precautionary statements

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.18800
Product name
Octanedioic acid
Purity
for synthesis
Packaging
100G
Price
$103
Updated
2024/03/01
Sigma-Aldrich
Product number
8.18800
Product name
Octanedioic acid
Purity
for synthesis
Packaging
500G
Price
$159
Updated
2024/03/01
Sigma-Aldrich
Product number
60930
Product name
Suberic acid
Purity
purum, ≥98.0% (T)
Packaging
100g
Price
$69
Updated
2024/03/01
Sigma-Aldrich
Product number
60930
Product name
Suberic acid
Purity
purum, ≥98.0% (T)
Packaging
1kg
Price
$280
Updated
2023/06/20
TCI Chemical
Product number
O0023
Product name
Suberic Acid
Purity
>99.0%(GC)(T)
Packaging
25g
Price
$19
Updated
2024/03/01
More
Less

Suberic acid Chemical Properties,Usage,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

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.

Uses

In the plastics industry.

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 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.]

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

Raw materials

Preparation Products

Hexamethylene Diisocyanate
More
Less

Suberic acid Suppliers

Americas 1 Belgium 3 Canada 1 China 361 Europe 3 Germany 14 India 41 Japan 7 Norway 1 Slovakia 1 South Korea 1 Sweden 1 Switzerland 5 Ukraine 2 United Kingdom 15 United States 49 USA 1 Global 507
HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Alfa Chemistry
Tel
1-516-6625404
Fax
1-516-927-0118
Email
support@alfa-chemistry.com
Country
United States
ProdList
9171
Advantage
60
AbaChemScene
Tel
732-484-9848
Fax
888-484-5008
Email
sales@chemscene.com
Country
United States
ProdList
3982
Advantage
60
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32161
Advantage
58
Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
TargetMol Chemicals Inc.
Tel
Email
support@targetmol.com
Country
United States
ProdList
38631
Advantage
58
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
Scandinavian Formulas
Tel
--
Fax
--
Email
mikep@scandinavianformulas.com
Country
United States
ProdList
1550
Advantage
58
Penta Manufacturing Company (a division of Penta International Corporation)
Tel
--
Fax
--
Email
@pentamfg.com
Country
United States
ProdList
901
Advantage
58
SGA Specialties Group, L.L.C.
Tel
--
Fax
--
Email
sales@sgaspecialties.com
Country
United States
ProdList
26
Advantage
58
Selleck Chemicals LLC
Tel
--
Fax
--
Email
sales@selleckchem.com
Country
United States
ProdList
1848
Advantage
58
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
MP Biomedicals, LLC. (Division of Valiant FC Co., Ltd.)
Tel
--
Fax
--
Email
serv@mpbio.com
Country
United States
ProdList
1854
Advantage
58
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United States
ProdList
4583
Advantage
58
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
VWR International, LLC.
Tel
--
Fax
--
Email
@sargentwelch.com
Country
United States
ProdList
6262
Advantage
58
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
Penta International Corporation
Tel
--
Fax
--
Email
lisaa@pentamfg.com
Country
United States
ProdList
5042
Advantage
58
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
MedChemExpress
Tel
--
Fax
--
Email
sales@medchemexpress.com
Country
United States
ProdList
6398
Advantage
58
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Anvia Chemicals, LLC
Tel
--
Fax
--
Email
sales@anviachem.com
Country
United States
ProdList
3933
Advantage
0
HBCChem Inc.
Tel
--
Fax
--
Email
sales@hbcchem-inc.com
Country
United States
ProdList
4569
Advantage
30
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
ChemService Inc.
Tel
--
Fax
--
Country
United States
ProdList
6379
Advantage
68
Dow Chemical Company
Tel
--
Fax
--
Email
dowcig@dow.com
Country
United States
ProdList
770
Advantage
90
INDOFINE Chemical Company, Inc.
Tel
--
Fax
--
Email
chemical@indofinechemical.com
Country
United States
ProdList
6176
Advantage
69
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
Narchem Corporation
Tel
--
Fax
--
Email
sales@narchem.com
Country
United States
ProdList
2813
Advantage
60
Penta Manufacturing Company
Tel
--
Fax
--
Email
sales@pentamfg.com
Country
United States
ProdList
5076
Advantage
65
Advanced Synthesis Technologies
Tel
--
Fax
--
Email
sales@advancedsynthesis.com
Country
United States
ProdList
4775
Advantage
61
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
United States
ProdList
6814
Advantage
81
Chem-Impex International, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6730
Advantage
64
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
City Chemical LLC
Tel
--
Fax
--
Email
sales@citychemical.com
Country
United States
ProdList
6708
Advantage
72
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
Pfaltz & Bauer, Inc.
Tel
--
Fax
--
Email
sales@pfaltzandbauer.com
Country
United States
ProdList
6828
Advantage
72
Davos Chemical Corporation
Tel
--
Fax
--
Email
info@davos.com
Country
United States
ProdList
1640
Advantage
65
Scandinavian Formulas, Inc.
Tel
--
Fax
--
Email
info@scandinavianformulas.com
Country
United States
ProdList
1447
Advantage
55
Eastern Chemical Corp.
Tel
--
Fax
--
Email
eastern@u-g.com
Country
United States
ProdList
2786
Advantage
34
City Chemicals Corporation
Tel
--
Fax
--
Country
United States
ProdList
6460
Advantage
72
Crescent Chemical Co., Inc.
Tel
--
Fax
--
Email
sales@creschem.com
Country
United States
ProdList
4597
Advantage
68
MP Biomedicals, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6561
Advantage
81
More
Less

View Lastest Price from Suberic acid manufacturers

Hebei Mujin Biotechnology Co.,Ltd
Product
Suberic acid 505-48-6
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-08-24
Hebei Weibang Biotechnology Co., Ltd
Product
Suberic acid 505-48-6
Price
US $1.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10 mt
Release date
2024-11-14
Honest Joy Holdings Limited
Product
Suberic acid 505-48-6
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100 tons
Release date
2022-07-05

505-48-6, Suberic acidRelated Search:

Sebacic acid Ethyl 2-(Chlorosulfonyl)acetate Azelaic acid Folic acid Suberic acid d,SUBERIC ACID DIETHYL ESTER Dibutyltin dilaurate SUBERIC ACID DIMETHYL ESTER Stearic acid Suberic acid 1-methyl ester,SUBERIC ACID MONOMETHYL ESTER,SUBERIC ACID METHYL ESTER Citric acid spiro[indene-1,4'-piperidine] hydrochloride SPIRO[INDENE-1,4'-PIPERIDINE] 1-Octanol Ascoric Acid DISUCCINIMIDYL SUBERATE BS3 dihexyl octanedioate octanedial

  • KORK ACID
  • Subericacid,99%
  • 142-144℃
  • octandioic acid
  • 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
  • CORK ACID
  • 1,6-Dicarboxyhexane
  • 1,8-Octanedioic acid
  • 1,8-octanedioicacid
  • Hexamethylenedicarboxylic acid
  • Octane-1,8-dioic acid
  • suberic
  • subericacid(octanedioicacid)
  • 1,6-HEXANEDICARBOXYLIC ACID
  • Oktanedioic acid
  • SUBERIC ACID
  • OCTANEDIOC ACID
  • OCTANEDIOIC ACID
  • SubericAcid&gt
  • suberate (octanedioate)
  • 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
  • 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
  • Lipids