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388378

Tributyl O-acetylcitrate

Name: Tributyl <I>O</I>-acetylcitrate
Brand: ALDRICH

98%

Synonym(s):

Tributyl 2-acetylcitrate, Acetyl tributyl citrate

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About This Item

Linear Formula:

CH₃CO₂C[CO₂(CH₂)₃CH₃][CH₂CO₂(CH₂)₃CH₃]₂

CAS Number:

77-90-7

Molecular Weight:

402.48

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24864222

EC Number:

201-067-0

Beilstein/REAXYS Number:

2303316

MDL number:

MFCD00043554

Assay:

98%

Form:

liquid

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Properties

Quality Level

100

vapor pressure

0.26 psi ( 20 °C), 0.8 psi ( 55 °C)

assay

98%

form

liquid

greener alternative product characteristics

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

sustainability

Greener Alternative Product

refractive index

n20/D 1.443 (lit.)

density

1.05 g/mL at 25 °C (lit.)

functional group

ester

greener alternative category

, Aligned

SMILES string

CCCCOC(=O)CC(CC(=O)OCCCC)(OC(C)=O)C(=O)OCCCC

InChI

1S/C20H34O8/c1-5-8-11-25-17(22)14-20(28-16(4)21,19(24)27-13-10-7-3)15-18(23)26-12-9-6-2/h5-15H2,1-4H3

InChI key

QZCLKYGREBVARF-UHFFFAOYSA-N

Description

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product is environmentally-benign and can replace highly toxic phthalates in membrane preparation and thus aligns with "Less Hazardous Chemical Syntheses". Click here for more information.

Application

Tributyl O-acetylcitrate (TBoAC) can be used:

As a plasticizer to improve flexibility and impact properties of polylactide (PLA) polymer.
As a processing additive for the formulation of bulk heterojunction (BHJ) polymeric organic solar cells (OSCs) to improve their efficiency.
In the preparation of semiconducting biopolymer composites of poly(3-hydroxy butyrate) (PHB).
In the synthesis of functionalized poly(vinyl chloride)(PVC) membranes for selective separation of perchlorate from water.

Storage Class

10 - Combustible liquids

flash_point_f

422.6 °F - closed cup

flash_point_c

217 °C - closed cup

ppe

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

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Guiding the selection of processing additives for increasing the efficiency of bulk heterojunction polymeric solar cells

Vongsaysy U, et al.

Advanced Energy Materials, 4(3), 1300752-1300752 (2014)

Higher dielectric properties of semiconducting biopolymer composites of poly (3-hydroxy butyrate)(PHB) with polyaniline (PANI), carbon black, and plasticizer

El-hadi AM, et al.

Polymer Bull., 75(4), 1681-1699 (2018)

Swelling of mucoadhesive electrospun chitosan/polyethylene oxide nanofibers facilitates adhesion to the sublingual mucosa.

Mai Bay Stie et al.

Carbohydrate polymers, 242, 116428-116428 (2020-06-23)

Mucoadhesive chitosan-based electrospun nanofibers are promising candidates for overcoming challenges associated with sublingual drug delivery, yet studies focusing on evaluating the mucoadhesive properties of nanofibers for sublingual administration are limited. The aim was to elucidate the mucoadhesive properties of chitosan/polyethylene

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Global Trade Item Number

SKU	GTIN
388378-500ML	04061831969221