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W201103

Sigma-Aldrich

Adipic acid

≥99.5%

Synonym(s):

Hexanedioic acid

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About This Item

Linear Formula:
HOOC(CH2)4COOH
CAS Number:
124-04-9
Molecular Weight:
146.14
FEMA Number:
2011
Beilstein/REAXYS Number:
1209788
EC Number:
204-673-3
Council of Europe no.:
26
MDL number:
MFCD00004420
UNSPSC Code:
12164502
eCl@ss:
39021711
PubChem Substance ID:
24900799
Flavis number:
8.026
NACRES:
NA.21

biological source

synthetic

reg. compliance

FDA 21 CFR 117

vapor density

5 (vs air)

vapor pressure

1 mmHg ( 159.5 °C)

assay

≥99.5%

autoignition temp.

788 °F

bp

265 °C/100 mmHg (lit.)

mp

151-154 °C (lit.)

solubility

H2O: soluble 23 g/L at 25 °C

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

odorless

SMILES string

OC(=O)CCCCC(O)=O

InChI

1S/C6H10O4/c7-5(8)3-1-2-4-6(9)10/h1-4H2,(H,7,8)(H,9,10)

InChI key

WNLRTRBMVRJNCN-UHFFFAOYSA-N

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pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H318

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCF8260
MKCH6431
MKCD9962
STBD4858V
STBB2946

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J B J H van Duuren et al.
Biotechnology and bioengineering, 108(6), 1298-1306 (2011-02-18)
A limited life cycle assessment (LCA) was performed on a combined biological and chemical process for the production of adipic acid, which was compared to the traditional petrochemical process. The LCA comprises the biological conversion of the aromatic feedstocks benzoic
Holger Noack et al.
Inorganic chemistry, 50(4), 1194-1202 (2011-01-28)
Adipic acid is a key compound in the chemical industry, where it is mainly used in the production of polymers. The conventional process of its generation requires vast amounts of energy and, moreover, produces environmentally deleterious substances. Thus, there is
H V Pawar et al.
Colloids and surfaces. B, Biointerfaces, 102, 102-110 (2012-09-26)
Streptomycin (STP) and diclofenac (DLF) loaded film dressings were prepared by blending Polyox(®) (POL) with four hydrophilic polymers [hydroxypropylmethylcellulose (HPMC), carrageenan (CAR), sodium alginate (SA) or chitosan (CS)] using glycerol (GLY) as plasticiser. The films were characterised by scanning electron
M A Shirai et al.
Carbohydrate polymers, 92(1), 19-22 (2012-12-12)
Biodegradable films were produced from blends contained a high amount of thermoplastic starch (TPS) and poly(lactic acid) (PLA) plasticized with different adipate or citrate esters. It was not possible to obtain pellets for the production of films using only glycerol
Krzysztof J Paluch et al.
Journal of pharmaceutical sciences, 100(8), 3268-3283 (2011-04-08)
The production of salt or cocrystalline forms is a common approach to alter the physicochemical properties of pharmaceutical compounds. The goal of this work was to evaluate the impact of anion choice (succinate, adipate, and sulfate) on the physicochemical characteristics
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