14079
コハク酸
ACS reagent grade, ≥99.5% (T), puriss. p.a.
別名:
ブタン二酸
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この商品について
化学式:
HOOCCH2CH2COOH
CAS番号:
分子量:
118.09
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
203-740-4
MDL number:
Beilstein/REAXYS Number:
1754069
Assay:
≥99.5% (T)
製品名
コハク酸, puriss. p.a., ACS reagent, ≥99.5% (T)
Quality Level
grade
ACS reagent, puriss. p.a.
assay
≥99.5% (T)
impurities
≤0.001% total nitrogen (N)
ign. residue
≤0.02%
bp
235 °C (lit.)
mp
184-186 °C (lit.), 185-191 °C
solubility
methanol: soluble 0.4 g/10 mL
anion traces
chloride (Cl-): ≤10 mg/kg, phosphate (PO43-): ≤10 mg/kg, sulfate (SO42-): ≤30 mg/kg
cation traces
Ca: ≤50 mg/kg, Cd: ≤5 mg/kg, Co: ≤5 mg/kg, Cr: ≤5 mg/kg, Cu: ≤5 mg/kg, Fe: ≤5 mg/kg, K: ≤50 mg/kg, Mg: ≤10 mg/kg, Mn: ≤5 mg/kg, Na: ≤50 mg/kg, Ni: ≤5 mg/kg, Pb: ≤5 mg/kg, Zn: ≤5 mg/kg
functional group
carboxylic acid
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
Application
Succinic acid may be employed in the following studies:
- Surfactant/detergent extender/foaming agent
- As ion chelator in the electroplating process
- As a precursor for various industrially important chemicals such as adipic acid, 1,4-butanediol, tetrahydrofuran, N-methyl pyrrolidinone, 2-pyrrolidinone, succinate salts, and γ-butyrolactone
- Synthesis of biodegradable polymers such as polybutyrate succinate (PBS) and polyamides.
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
保管分類
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
P C Lee et al.
Biotechnology and bioengineering, 72(1), 41-48 (2000-11-21)
Succinic acid was produced by fermentation of Anaerobiospirillum succiniciproducens using glycerol as a carbon source. When cells were anaerobically cultured in a medium containing 6.5 g/L glycerol, a high succinic acid yield (133%) was obtained while avoiding the formation of
Biotechnology of succinic acid production and markets for derived industrial products.
Zeikus JG, et al.
Applied Microbiology and Biotechnology, 51(5), 545-552 (1999)
Virendra Gajbhiye et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 48(4-5), 668-679 (2013-01-10)
The present investigation was aimed at exploring dual targeting of anti-HIV drug, zidovudine (ZDV) via sialic acid conjugated-mannosylated poly(propyleneimine) (PPI) dendritic nano-constructs. Fourth generation PPI dendrimers, sialic acid conjugated PPI dendrimers (SPPI), mannose conjugated PPI dendrimers (MPPI) and dual ligand