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27500

Sigma-Aldrich

Triethyl citrate

greener alternative

≥98.0% (GC)

Sinônimo(s):

Ethyl citrate

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About This Item

Fórmula linear:
HOC(COOC2H5)(CH2COOC2H5)2
Número CAS:
77-93-0
Peso molecular:
276.28
Beilstein:
1801199
Número CE:
201-070-7
Número MDL:
MFCD00009201
Código UNSPSC:
12352100
ID de substância PubChem:
57648253
NACRES:
NA.22

densidade de vapor

9.7 (vs air)

pressão de vapor

1 mmHg ( 107 °C)

Ensaio

≥98.0% (GC)

forma

liquid

características do produto alternativo mais ecológico

Less Hazardous Chemical Syntheses
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

índice de refração

n20/D 1.442 (lit.)

pb

235 °C/150 mmHg (lit.)

densidade

1.14 g/mL at 25 °C (lit.)

categoria alternativa mais ecológica

, Aligned

cadeia de caracteres 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

chave InChI

DOOTYTYQINUNNV-UHFFFAOYSA-N

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Descrição geral

Triethyl citrate is a safe direct food additive.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product can replace highly toxic diluents in membrane preparation and thus aligns with "Less Hazardous Chemical Syntheses". Click here for more information.

Aplicação

Triethyl citrate was used as a plasticizer in the study of the feasibility of near-infrared (NIR) spectroscopy in determining the influence of plasticizer levels and sintering temperature on the breaking force of extended-release matrix tablets prepared by roller-compaction.

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

311.0 °F - closed cup

Ponto de fulgor (°C)

155 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Sigma-Aldrich

8.20350

Tributyl citrate

Tributyl 2-acetylcitrate ≥98%, FG

Sigma-Aldrich

W308005

Tributyl 2-acetylcitrate

Triethyl 2-acetylcitrate Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1157

Triethyl 2-acetylcitrate

Dibutyl sebacate ≥97.0% (GC)

Sigma-Aldrich

84840

Dibutyl sebacate

Monice M Fiume et al.
International journal of toxicology, 33(2 suppl), 16S-46S (2014-05-28)
The CIR Expert Panel (Panel) assessed the safety of citric acid, 12 inorganic citrate salts, and 20 alkyl citrate esters as used in cosmetics, concluding that these ingredients are safe in the present practices of use and concentration. Citric acid
Vivek S Dave et al.
Drug development and industrial pharmacy, 41(6), 898-905 (2014-05-03)
The aim of this study was to investigate the feasibility of near-infrared (NIR) spectroscopy for the determination of the influence of sintering temperature and plasticizer levels on the breaking force of extended-release matrix tablets prepared via roller-compaction. Six formulations using
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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