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09582

Sigma-Aldrich

Adipic acid

BioXtra, ≥99.5% (HPLC)

Sinónimos:

Hexanedioic acid

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About This Item

Fórmula lineal:
HOOC(CH2)4COOH
Número de CAS:
124-04-9
Peso molecular:
146.14
Beilstein/REAXYS Number:
1209788
EC Number:
204-673-3
MDL number:
MFCD00004420
UNSPSC Code:
12352106
eCl@ss:
39021711
PubChem Substance ID:
329748777
NACRES:
NA.21

vapor density

5 (vs air)

Quality Level

200

vapor pressure

1 mmHg ( 159.5 °C)

product line

BioXtra

assay

≥99.5% (HPLC)

autoignition temp.

788 °F

ign. residue

≤0.05% (as SO4)

loss

≤1% loss on drying, 110 °C

bp

265 °C/100 mmHg (lit.)

mp

151-154 °C (lit.)
151-154 °C

solubility

H2O: soluble 23 g/L at 25 °C

anion traces

chloride (Cl-): ≤50 mg/kg
nitrate (NO3-): ≤30 mg/kg
sulfate (SO42-): ≤500 mg/kg

cation traces

As: ≤3 mg/kg
Cu: ≤10 mg/kg
Fe: ≤5 mg/kg
Pb: ≤10 mg/kg
Zn: ≤10 mg/kg

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Hydriodic acid contains no stabilizer, distilled, 57 wt. % in H2O, 99.99% trace metals basis

Sigma-Aldrich

210013

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Ácido succínico BioXtra, BioRenewable, ≥99.0%

Sigma-Aldrich

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o-Xylene puriss. p.a., ≥99.0% (GC)

Sigma-Aldrich

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Sigma-Aldrich

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Roohan Rakhshaee et al.
Journal of hazardous materials, 189(1-2), 158-166 (2011-03-15)
The removal of methylene blue (MB) as a cationic dye from aqueous solution by the stabilized Fe(3)O(4) nano-particles with the extracted pectin from apple waste (FN-PA) increased due to using the cross-linked forms of the bound pectin on the nano-particles
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
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
Tânia Veiga et al.
Metabolic engineering, 14(4), 437-448 (2012-04-25)
Industrial production of semi-synthetic cephalosporins by Penicillium chrysogenum requires supplementation of the growth media with the side-chain precursor adipic acid. In glucose-limited chemostat cultures of P. chrysogenum, up to 88% of the consumed adipic acid was not recovered in cephalosporin-related
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