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W308307

Sigma-Aldrich

Triethyl citrate

≥99%, FCC, FG

Synonyme(s) :

Ethyl citrate

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About This Item

Formule linéaire :
HOC(COOC2H5)(CH2COOC2H5)2
Numéro CAS:
Poids moléculaire :
276.28
Numéro FEMA:
3083
Numéro Beilstein :
1801199
Numéro CE :
Conseil de l'Europe Nº :
11762
Numéro MDL:
Code UNSPSC :
12164502
ID de substance PubChem :
Numéro Flavis :
9.512
Nomenclature NACRES :
NA.21

Source biologique

synthetic

Niveau de qualité

Qualité

FG
Halal
Kosher

Agence

meets purity specifications of JECFA

Conformité réglementaire

EU Regulation 1334/2008 & 872/2012
FCC
FDA 21 CFR 117
FDA 21 CFR 175.300
FDA 21 CFR 175.320
FDA 21 CFR 181.27
FDA 21 CFR 184.1911

Densité de vapeur

9.7 (vs air)

Pression de vapeur

1 mmHg ( 107 °C)

Pureté

≥99%

Indice de réfraction

n20/D 1.442 (lit.)

Point d'ébullition

235 °C/150 mmHg (lit.)

Densité

1.14 g/mL at 25 °C (lit.)

Application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

Allergène alimentaire

no known allergens

Propriétés organoleptiques

odorless

Chaîne SMILES 

CCOC(=O)CC(O)(CC(=O)OCC)C(=O)OCC

InChI

1S/C12H20O7/c1-4-17-9(13)7-12(16,11(15)19-6-3)8-10(14)18-5-2/h16H,4-8H2,1-3H3

Clé InChI

DOOTYTYQINUNNV-UHFFFAOYSA-N

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Description générale

Triethyl citrate can be used as a plasticizer and sequestrant in the food industry.

Application


  • Cosmetically Approved Short-Chain Alcohol/Triethyl Citrate/Water Surfactant-Free Microemulsions and Potential Application to Transdermal Penetration of α-Arbutin.: This study investigates the formulation of surfactant-free microemulsions using triethyl citrate, exploring its potential in enhancing the transdermal penetration of α-arbutin. The results suggest significant improvement in skin delivery, highlighting the cosmetic and pharmaceutical potential of triethyl citrate (Zhang et al., 2024).

  • Understanding the Interaction of Thermal, Rheological, and Mechanical Parameters Critical for the Processability of Polyvinyl Alcohol-Based Systems during Hot Melt Extrusion.: This research delves into the role of triethyl citrate as a plasticizer in polyvinyl alcohol-based systems, essential for optimizing hot melt extrusion processes. The findings emphasize the importance of precise thermal and mechanical control in pharmaceutical applications (Hess et al., 2024).

  • The effect of additives on the biodegradation of polyhydroxyalkanoate (PHA) in marine field trials.: Triethyl citrate is evaluated as an additive to improve the biodegradation of polyhydroxyalkanoates in marine environments. This study presents its efficacy in enhancing environmental sustainability through accelerated degradation (Read et al., 2024).

  • In-situ forming PLGA implants: Towards less toxic solvents.: Investigating the use of triethyl citrate as a less toxic solvent alternative in PLGA implants, this paper demonstrates its potential in reducing toxicity while maintaining implant efficacy, beneficial for pharmaceutical applications (Ramos et al., 2024).

  • Influence of Low-Molecular-Weight Esters on Melt Spinning and Structure of Poly(lactic acid) Fibers.: This article explores the impact of triethyl citrate on the properties of poly(lactic acid) fibers, highlighting its role in enhancing fiber structure and processability for industrial applications (Gzyra-Jagieła et al., 2024).

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

311.0 °F - closed cup

Point d'éclair (°C)

155 °C - closed cup

Équipement de protection individuelle

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


Certificats d'analyse (COA)

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Dictionary of Food ingredients, 144-144 (2013)
Food Additives, 682-682 (1999)
M R Abbaspour et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 68(3), 747-759 (2007-11-06)
One challenge in tableting of sustained-release multiparticulates is maintaining the desired drug release after compaction. The aim of this study was to design sustained-release ibuprofen tablets which upon oral ingestion rapidly disintegrate into sustained-release pellets in which the integrity of
Soravoot Rujivipat et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 81(1), 223-229 (2012-01-25)
Enteric polymers such as cellulose esters (cellulose acetate phthalate, hydroxypropylmethylcellulose acetate succinate) and methacrylic acid-acrylate copolymers (Eudragit® L100-55 and S100) are quite brittle in the dry state and thus not suitable as pellet coatings for compression into tablets. The objective
Kakuyou Ogawa et al.
Biological & pharmaceutical bulletin, 37(9), 1559-1563 (2014-09-02)
Zerumbone 1 is an 11-membered cyclic sesquiterpene obtained from the rhizomes of Zingiber zerumbet SMITH (Zingiberaceae). In this study, we investigated the structure-activity relationship of 1, α-humulene (2), tetrahydrozerumbone stereoisomers (3-5), and tetrahydrozerumbone derivatives (6-9). The oxygen-containing functional groups and

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