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About This Item
Linear Formula:
HOOC(CH2)4COOH
CAS Number:
Molecular Weight:
146.14
NACRES:
NA.21
PubChem Substance ID:
eCl@ss:
39021711
UNSPSC Code:
12352106
EC Number:
204-673-3
MDL number:
Beilstein/REAXYS Number:
1209788
Product Name
Adipic acid, 99%
InChI key
WNLRTRBMVRJNCN-UHFFFAOYSA-N
InChI
1S/C6H10O4/c7-5(8)3-1-2-4-6(9)10/h1-4H2,(H,7,8)(H,9,10)
SMILES string
OC(=O)CCCCC(O)=O
vapor density
5 (vs air)
vapor pressure
1 mmHg ( 159.5 °C)
assay
99%
form
solid
autoignition temp.
788 °F
bp
265 °C/100 mmHg (lit.)
mp
151-154 °C (lit.)
solubility
H2O: soluble 23 g/L at 25 °C
Quality Level
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Related Categories
Application
Adipic acid can be used as a starting material in the preparation of:
- Aliphatic polyesters by reacting with ethyleneglycol/1,3 propyleneglycol/1,4-butanediol using inorganic acid as a catalyst.
- Cyclopentanone using a weak base such as Na2CO3.
- Linear polybutylene adipate (PBA) having carboxylic acids at the terminals by reacting with 1,4-butanediol.
General description
Adipic acid is a straight-chain aliphatic dicarboxylic acid, commonly used in the manufacturing of nylon-6,6 and plasticizers. Conventionally it was manufactured from petrochemicals but in recent days it can be synthesized from renewable substrates by means of biological methods.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
384.8 °F - closed cup
flash_point_c
196 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Ketonic decarboxylation catalysed by weak bases and its application to an optically pure substrate
Renz M and Corma A
European Journal of Organic Chemistry, 2004(9), 2036-2039 (2004)
Synthesis of aliphatic polyesters by polycondensation using inorganic acid as catalyst
Sokolsky-Papkov M, et al.
Polymers For Advanced Technologies, 22(5), 502-511 (2011)
Biological production of adipic acid from renewable substrates: Current and future methods
Deng Y, et al.
Biochemical Engineering Journal, 105, 16-26 (2016)
Migration resistant polymeric plasticizer for poly (vinyl chloride)
Lindstrom A and Hakkarainen M
Journal of Applied Polymer Science, 104(4), 2458-2467 (2007)
Synthesis and characterization of high molecular weight branched PBA
Han Y, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 39(13), 2143-2150 (2001)
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