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Merck
CN

D1009

Dodecanedioic acid

99%

Synonym(s):

Decane-1,10-dicarboxylic acid

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About This Item

Linear Formula:
HOOC(CH2)10COOH
CAS Number:
693-23-2
Molecular Weight:
230.30
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24893317
EC Number:
211-746-3
Beilstein/REAXYS Number:
1782580
MDL number:
MFCD00002735

Key Documents

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Product Name

Dodecanedioic acid, 99%

InChI key

TVIDDXQYHWJXFK-UHFFFAOYSA-N

InChI

1S/C12H22O4/c13-11(14)9-7-5-3-1-2-4-6-8-10-12(15)16/h1-10H2,(H,13,14)(H,15,16)

SMILES string

OC(=O)CCCCCCCCCCC(O)=O

vapor pressure

21 mmHg ( 222 °C)

assay

99%

form

pellets

bp

245 °C/10 mmHg (lit.)

mp

127-129 °C (lit.)

Quality Level

100

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Application

Dodecanedioic acid can be used as a reactant in the:
  • Solvent-free synthesis of biobased polyester polyols by reacting with 1,4-pentanediol.
  • Arylboronic acid-catalyzed direct condensation with ureas to synthesize N,N′-diacyl-2-imidazolidones.
It can also be used as a catalyst for the allylation of benzoquinones to synthesize lapachol using allyl alcohols or acetates.

General description

Dodecanedioic acid (DDA) is a medium-chaindicarboxylic fatty acid commonly used in the production of polyamidenylon-6,12. This material is recognized for its resistance to heat andchemicals, making it suitable for various technical applications, such as heatand chemical-resistant sheaths.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk

nwg

flash_point_f

428.0 °F - closed cup

flash_point_c

220 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW0006
MKCV2133
MKCR7145
MKBF2637
MKBD8809

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Lieven Van Meulebroek et al.
Analytical chemistry, 89(22), 12502-12510 (2017-10-21)
As lipids are assigned a plethora of biological functions, it is evident that dysregulated lipid metabolism signifies a key element in many pathological conditions. With this rationale, this study presents a validated lipidomics platform to map the fecal lipidome, which
Harsha Ramaraju et al.
PloS one, 15(2), e0229112-e0229112 (2020-02-23)
Development of biodegradable shape memory elastomers (SMEs) is driven by the growing need for materials to address soft tissue pathology using a minimally invasive surgical approach. Composition, chain length and crosslinking of biocompatible polymers like PCL and PLA have been
Christopher J van der Gast et al.
Environmental microbiology, 6(3), 254-263 (2004-02-12)
In order for established bioreactors to be effective for treating chemically mixed wastes such as metal working fluids (MWF) it is essential that they harbour microbial populations that can maintain sufficient active biomass and degrade each of the chemical constituents
Susanne Ditlevsen et al.
Bulletin of mathematical biology, 67(3), 547-561 (2005-04-12)
Deterministic and stochastic differential equations models of the uptake of dodecanedioic acid (C12) are fitted to experimental data obtained on nine isolated, perfused rat livers. 11500 mug of C12 were injected as a bolus into the perfusing liver solution. The
Stanley H Korman et al.
Molecular genetics and metabolism, 86(3), 337-343 (2005-09-09)
Detection of hepatic carnitine palmitoyltransferase I (CPT IA) deficiency by metabolite screening may be problematic. The urine organic acid profile is generally said to be normal and no abnormal or increased acylcarnitine species are evident on bloodspot tandem MS examination.
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