P45001
Pimelic acid
98%
Synonim(y):
Heptanedioic acid
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About This Item
Wzór liniowy:
HO2C(CH2)5CO2H
Numer CAS:
Masa cząsteczkowa:
160.17
Beilstein:
1210024
Numer WE:
Numer MDL:
Kod UNSPSC:
12352100
Identyfikator substancji w PubChem:
NACRES:
NA.22
Próba
98%
Postać
crystals
tw
212 °C/10 mmHg (lit.)
mp
103-105 °C (lit.)
ciąg 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)
Klucz InChI
WLJVNTCWHIRURA-UHFFFAOYSA-N
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Opis ogólny
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.
Zastosowanie
- 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).
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Hasło ostrzegawcze
Warning
Zwroty wskazujące rodzaj zagrożenia
Zwroty wskazujące środki ostrożności
Klasyfikacja zagrożeń
Eye Irrit. 2 - STOT SE 3
Organy docelowe
Respiratory system
Kod klasy składowania
11 - Combustible Solids
Klasa zagrożenia wodnego (WGK)
WGK 2
Temperatura zapłonu (°F)
Not applicable
Temperatura zapłonu (°C)
Not applicable
Środki ochrony indywidualnej
dust mask type N95 (US), Eyeshields, Gloves
Certyfikaty analizy (CoA)
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Klienci oglądali również te produkty
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
V G Mahadevappa et al.
Biochimica et biophysica acta, 713(1), 73-79 (1982-10-14)
The molecular species composition of the individual diacyl phospholipids was determined in human platelets. The 1-acyl (16:0, 18:0, etc.) homologues of the various 2-acyl (16:0, 18:1, 18:2, 20:4, etc) species of the phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine and phosphatidylinositol were assessed by
S Passi et al.
Acta dermato-venereologica. Supplementum, 143, 8-13 (1989-01-01)
Medium chain length dicarboxylic acids (DA) from C8 to C13 are competitive inhibitors of tyrosinase in vitro. The introduction of electron acceptor groups or electron donor groups into the 2 and/or the 8 position of the molecule enhances or reduces
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
Concentrations of riboflavin and related organic acids in children with protein-energy malnutrition.
C D Capo-Chichi et al.
The American journal of clinical nutrition, 71(4), 978-986 (2000-03-25)
Riboflavin, flavin mononucleotide (FMN), and flavin adenine dinucleotide (FAD) concentrations have been little studied in cases of malnutrition. Our objective was to investigate the effects of malnutrition on riboflavin status and riboflavin's relation with thyroid hormones and concentrations of urinary
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