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trans-Aconitic acid

Name: <I>trans</I>-Aconitic acid
Brand: ALDRICH

98%

Sinonimo/i:

trans-Propene-1,2,3-tricarboxylic acid

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About This Item

Formula condensata:

HO₂CCH₂C(CO₂H)=CHCO₂H

Numero CAS:

4023-65-8

Peso molecolare:

174.11

Beilstein:

1725830

Numero CE:

223-688-6

Numero MDL:

MFCD00002721

Codice UNSPSC:

12352100

ID PubChem:

24847505

NACRES:

NA.22

Saggio

98%

Forma fisica

solid

Punto di fusione

190 °C (dec.) (lit.)

Stringa SMILE

OC(=O)C\C(=C/C(O)=O)C(O)=O

InChI

1S/C6H6O6/c7-4(8)1-3(6(11)12)2-5(9)10/h1H,2H2,(H,7,8)(H,9,10)(H,11,12)/b3-1+
GTZCVFVGUGFEME-HNQUOIGGSA-N

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Descrizione generale

trans-Aconitic acid is inhibitor of the tricarboxylic acid cycle and was identified in range grasses.

trans-Aconitic acid is an antioxidant used in food and cosmetics preparation and also used as a plasticizer in the polymer industry.

Applicazioni

trans-Aconitic acid was used in synthesis of aconitate esters. It may be used for cross-linking polyvinyl alcohol film for preparing composite nanofiltration membranes.

Azioni biochim/fisiol

Antimicrobial agent that blocks the transformation of Leishmania donovani amastigotes to prostigotes.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Sigma-Aldrich

I16005

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Sigma-Aldrich

259926

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Effect of Cross-Linking Agent Chemistry and Coating Conditions on Physical, Chemical and Separation Properties of PVA-PSf Composite Membranes.

Dlamini DS, et al. et al.

Separation Science and Technology (2013)

Effect of catalytic conditions on the synthesis of new aconitate esters.

Piang-Siong W, et al.

Industrial Crops and Products, 35(1), 203-210 (2012)

Trans-Aconitic Acid in Range Grasses in Early Spring.

R Burau et al.

Science (New York, N.Y.), 150(3697), 766-767 (1965-11-05)

trans-Aconitate ion, an inhibitor of the tricarboxylic acid cycle, was identified in range grasses as trans-aconitic acid, which was isolated in crystalline form. It occurs in surprisingly high concentrations in early-season forage grasses. Dry-weight concentrations of trans-aconitate vary with season

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Physiological and morphological adaptations of herbaceous perennial legumes allow differential access to sources of varyingly soluble phosphate.

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