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Undecanedioic acid

CAS No.
1852-04-6
Chemical Name:
Undecanedioic acid
Synonyms
Undecanedionic acid;IRGACORDC11;Pure Mix II;undecanedioate;undecane diacid;Tridecanediamine;undecandioic acid;UNDECANEDIOIC ACID;RARECHEM AL BO 0436;HENDECANEDIOIC ACID
CBNumber:
CB6424163
Molecular Formula:
C11H20O4
Molecular Weight:
216.27
MDL Number:
MFCD00004444
MOL File:
1852-04-6.mol
MSDS File:
SDS
Last updated:2023-11-20 10:16:26

Undecanedioic acid Properties

Melting point 108-110 °C (lit.)
Boiling point 389.33°C (rough estimate)
Density 1.1629 (rough estimate)
vapor pressure 10Pa at 20℃
refractive index 1.4421 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility methanol: 10 mg/mL, clear
form Solid
pka 4.48±0.10(Predicted)
color White to Off-White
Water Solubility 5.10g/L(21 ºC)
BRN 1780537
InChIKey LWBHHRRTOZQPDM-UHFFFAOYSA-N
LogP 2.8 at 25℃
CAS DataBase Reference 1852-04-6(CAS DataBase Reference)
FDA UNII 7059GFK8NV
NIST Chemistry Reference Undecanedioic acid(1852-04-6)
EPA Substance Registry System Undecanedioic acid (1852-04-6)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
HS Code  29171900
NFPA 704
0
2 0

Undecanedioic acid price More Price(31)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 177962 Undecanedioic acid 97% 1852-04-6 1g $171 2024-03-01 Buy
TCI Chemical N0333 1,9-Nonanedicarboxylic Acid >97.0%(GC)(T) 1852-04-6 5g $172 2024-03-01 Buy
TCI Chemical N0333 1,9-Nonanedicarboxylic Acid >97.0%(GC)(T) 1852-04-6 25g $572 2024-03-01 Buy
TRC U787780 Undecanedioic acid 1852-04-6 1g $85 2021-12-16 Buy
AK Scientific N008 Undecanedioic acid 1852-04-6 25g $134 2021-12-16 Buy
Product number Packaging Price Buy
177962 1g $171 Buy
N0333 5g $172 Buy
N0333 25g $572 Buy
U787780 1g $85 Buy
N008 25g $134 Buy

Undecanedioic acid Chemical Properties,Uses,Production

Description

Undecanedioic acid, in the form of a white powder or flake, is dibasic acids which is a family of organic compounds, also known as ‘long-chain dicarboxylic acids’. Undecanedioic acid is an alpha, omega-dicarboxylic acid that is nonane with two carboxylic acid groups at positions C-1 and C-9. It has a role as a metabolite. It is a conjugate acid of an undecanedioic acid anion. It has recommended applications in corrosion inhibitors, hot melt adhesives, high performance polyamides/nylon, metal-working fluid, lubircant, adhesive, powder coating, and more. 
Undecanedioic acid has been found in parts of human aortas with advanced atherosclerotic lesions associated with intercellular matrix macromolecules and specifically with elastin, and may be the result of an increased hydrolysis of esters and (or) a decreased esterification. Undecanedioic acid has been found (among other unusual dicarboxylic acids) in the urine from patients under hopantenate therapy during episodes of Reye's-like syndrome.

Chemical Properties

white to light yellow powder

Uses

Undecanedioic Acid is a bioactive compound found in Polygala tenuifolia root which is used as a functional food due to its attractive health benefits.

Definition

ChEBI: An alpha,omega-dicarboxylic acid that is nonane with two carboxylic acid groups at positions C-1 and C-9.

Flammability and Explosibility

Non flammable

Synthesis

Undecanedioic acid is obtained by reacting α -nitro ketone and NaOH in MeOH.To a solution of α -nitro ketone (0.7 mmol) in MeOH (4.2 ml), 25 ml of 0.5 M Na2HPO4 in a 1 N of NaOH were added and the resulting mixture was heated at 70 °C for 1-4 h, then Oxone (1.75 mmol) in water (3 ml) was added to the cold solution (r. t.). After 4 h the mixture was diluted with brine (10 ml), acidified to pH=2 with a 10% solution of HCl and extracted with EtOAc (3 x 20 ml). The combined organic layers were washed with brine (10 ml), dried over Na2SO4 and evaporated to yield pure dicarboxylic acid.
synthetic method of Undecanedioic acid
Fig The synthetic method 2 of Undecanedioic acid.

Source

Undecanedioic acid is a natural product found in Aloe africana, Phaseolus vulgaris, and other organisms with data available.

1092935-24-4
1852-04-6
Synthesis of Undecanedioic acid from 2-Undecenedioic acid, 1-methyl ester

Undecanedioic acid Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 304)Suppliers
Supplier Tel Email Country ProdList Advantage
Xiamen AmoyChem Co., Ltd
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View Lastest Price from Undecanedioic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Undecanedioic acid pictures 2023-10-16 Undecanedioic acid
1852-04-6
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
Undecanedioic acid pictures 2023-09-06 Undecanedioic acid
1852-04-6
US $0.00 / KG 1KG 99% 500000kg Hebei Guanlang Biotechnology Co., Ltd.
Undecanedioic acid pictures 2022-10-19 Undecanedioic acid
1852-04-6
US $100.00 / kg 1kg 0.99 100 tons Hebei Duling International Trade Co. LTD
Nonane-1,9-dicarboxylic acid Undecanedioic acid,97% Nonamethylenedicarboxylic Acid Undecanedioic Acid Undecanedioic acid,1,9-Nonanedicarboxylic acid Undecane-1,11-dioic acid UNDECANEDIOIC ACID RARECHEM AL BO 0436 NONAMETHYLENEDICARBOXYLIC ACID 1,11-UNDECANEDIOIC ACID 1,9-NONAMETHYLENE DICARBOXYLIC ACID 1,9-NONANEDICARBOXYLIC ACID HENDECANEDIOIC ACID DICARBOXYLIC ACID C11 undecandioic acid undecane diacid UNDECANEDIOIC ACID 97% DC11(Undecanedioic Acid) IRGACORDC11 nonanedicarboxylic acid Undecanedioic acid UDDA 1,9-NonanedicarboxylicAcid> Fourteen carbon dibasic acid undecanedioate Lauryl polyoxyethylene ether sulfosuccinate monosodium disodium TIANFU CHEM--Undecanedioic acid Undecanedionic acid Tridecanediamine Pure Mix II 1852-04-6 HOOCCH29COOH C9H19COOH2 C9H18COOH2 C11 to C12 Carboxylic Acids Carbonyl Compounds Building Blocks Organic Building Blocks Monofunctional & 伪,蠅-Bifunctional Alkanes 伪,蠅-Bifunctional Alkanes 伪,蠅-Alkanedicarboxylic Acids Undecanedionic acid Building Blocks C11 to C12 Carbonyl Compounds Carboxylic Acids Chemical Synthesis Organic Building Blocks Monofunctional & alpha,omega-Bifunctional Alkanes alpha,omega-Alkanedicarboxylic Acids alpha,omega-Bifunctional Alkanes