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14080

Sigma-Aldrich

Succinic acid

purum p.a., ≥99.0% (T)

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Synonym(s):
Butanedioic acid
Linear Formula:
HOOCCH2CH2COOH
CAS Number:
Molecular Weight:
118.09
Beilstein:
1754069
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.21

grade

purum p.a.

Quality Level

Assay

≥99.0% (T)

ign. residue

≤0.05% (as SO4)

bp

235 °C (lit.)

mp

184-186 °C (lit.)
185-188 °C

solubility

methanol: soluble 0.4 g/10 mL

anion traces

chloride (Cl-): ≤50 mg/kg
sulfate (SO42-): ≤100 mg/kg

cation traces

Ca: ≤50 mg/kg
Cd: ≤50 mg/kg
Co: ≤50 mg/kg
Cu: ≤50 mg/kg
Fe: ≤50 mg/kg
K: ≤100 mg/kg
Na: ≤100 mg/kg
Ni: ≤50 mg/kg
Pb: ≤50 mg/kg
Zn: ≤50 mg/kg

SMILES string

OC(=O)CCC(O)=O

InChI

1S/C4H6O4/c5-3(6)1-2-4(7)8/h1-2H2,(H,5,6)(H,7,8)

InChI key

KDYFGRWQOYBRFD-UHFFFAOYSA-N

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This Item
14079S7501398055
Succinic acid purum p.a., ≥99.0% (T)

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14080

Succinic acid

Succinic acid puriss. p.a., ACS reagent, ≥99.5% (T)

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14079

Succinic acid

Succinic acid ReagentPlus®, BioRenewable, ≥99.0%

Sigma-Aldrich

S7501

Succinic acid

Succinic acid ACS reagent, ≥99.0%

Sigma-Aldrich

398055

Succinic acid

assay

≥99.0% (T)

assay

≥99.5% (T)

assay

≥99.0%

assay

≥99.0%

bp

235 °C (lit.)

bp

235 °C (lit.)

bp

235 °C (lit.)

bp

235 °C (lit.)

mp

184-186 °C (lit.), 185-188 °C

mp

184-186 °C (lit.), 185-191 °C

mp

184-186 °C (lit.)

mp

184-186 °C (lit.)

solubility

methanol: soluble 0.4 g/10 mL

solubility

methanol: soluble 0.4 g/10 mL

solubility

H2O: soluble 1 g/10 mL

solubility

water: soluble 83 g/L at 25 °C

anion traces

chloride (Cl-): ≤50 mg/kg, sulfate (SO42-): ≤100 mg/kg

anion traces

chloride (Cl-): ≤10 mg/kg, phosphate (PO43-): ≤10 mg/kg, sulfate (SO42-): ≤30 mg/kg

anion traces

-

anion traces

chloride (Cl-): ≤0.001%, phosphate (PO43-): ≤0.001%, sulfate (SO42-): ≤0.003%

Application

Succinicacid can be used as an organic additive in the synthesis of:
  • 2-Benzyl substituted isoquinoline N-oxides by rhodium-catalyzed reaction with aryl oximes and secondary propargyl alcohols.
  • Spiro-pyrimidine derivatives by cyclization reaction of 5-(2-alkohybenzylidene) barbituric acid.
  • Allylselenol via reduction of allyl selenocyanate using lithium aluminum hydride.
It can also be used as a reactant to synthesize:
  • Polyesters via catalyst-free polyesterification of glycerol and azelaic acid.
  • Poly(glycerol-succinic acid) biodendrimers applicable in specific medical and biotechnological uses.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Rhodium-Catalyzed C- H Activation/Annulation Cascade of Aryl Oximes and Propargyl Alcohols to Isoquinoline N-Oxides
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