P45001
Pimelic acid
98%
Sinônimo(s):
Heptanedioic acid
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About This Item
Fórmula linear:
HO2C(CH2)5CO2H
Número CAS:
Peso molecular:
160.17
Beilstein:
1210024
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Formulário:
crystals
Ensaio:
98%
Produtos recomendados
Nível de qualidade
Ensaio
98%
Formulário
crystals
p.e.
212 °C/10 mmHg (lit.)
pf
103-105 °C (lit.)
cadeia de caracteres SMILES
OC(=O)CCCCCC(O)=O
InChI
1S/C7H12O4/c8-6(9)4-2-1-3-5-7(10)11/h1-5H2,(H,8,9)(H,10,11)
chave InChI
WLJVNTCWHIRURA-UHFFFAOYSA-N
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Descrição geral
Pimelic acid, also known as heptanedioic acid, is a dicarboxylic acid commonly used as a precursor in the biosynthesis of biotin. It serves as a building block in the synthesis of various compounds , and it is used as a key precursor in the production of polyamides, polyesters, and other polymers.
Aplicação
- Pimelic acid in microbial soil treatments: A 2023 study examined the use of pimelic acid in soil treatment, observing its impact on the microbial community structure and metabolites in bayberry plantations. This application illustrates its potential in agricultural biotechnology and soil remediation (Ren et al., 2023).
- Pharmaceutical applications of pimelic acid: A 2023 study involved pimelic acid in the preparation and physiochemical analysis of novel ciprofloxacin/dicarboxylic acid salts, showcasing its utility as a pharmaceutical intermediate (Hibbard et al., 2023).
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Van Velthoven et al.
European Polymer Journal, 66, 57-66 (2015)
Kilogram Synthesis of Crebinostat
Yongjun et al.
Synthesis and Chemistry of Agrochemicals V, 48 (2016)
Pimelic acid, the first precursor of the B acillus subtilis biotin synthesis pathway, exists as the free acid and is assembled by fatty acid synthesis
Manandhar et al.
Molecular Microbiology, 104, 595-607 (2017)
T Niwa et al.
Clinica chimica acta; international journal of clinical chemistry, 99(1), 71-83 (1979-11-15)
(1) 2,4-Dimethyladipic acid was first identified in normal human urine using gas chromatography-mass spectrometry. Urinary excretion of 2,4-dimethyladipic acid in 7 healthy adults ranged from 4.9 mumol to 14 mumol per 24 h. (2) Succinic acid, adipic acid, 3-methyladipic acid
B R Pettit
Clinica chimica acta; international journal of clinical chemistry, 156(1), 85-90 (1986-04-15)
A selected ion monitoring assay for thiodiglycollic acid in urine is described. Urine samples are analysed by combined gas chromatography-mass spectrometry as their dibutyl esters using pimelic acid as an internal standard. Rapid analysis was achieved by the simplification of
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