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796832

Sigma-Aldrich

Phthalic acid mono-2-ethylhexyl ester

97%

Sinonimo/i:

mono-2-Ethylhexyl phthalate

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About This Item

Formula empirica (notazione di Hill):
C16H22O4
Numero CAS:
Peso molecolare:
278.34
Beilstein:
3206630
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Descrizione

Flash Point: >110°C

Livello qualitativo

Saggio

97%

Stato

liquid (Colorless)

Indice di rifrazione

n/D 1.5051

Densità

1.0864 g/mL at 25 °C

Gruppo funzionale

carboxylic acid
ester

Stringa SMILE

O=C(O)C1=CC=CC=C1C(OCC(CC)CCCC)=O

InChI

1S/C16H22O4/c1-3-5-8-12(4-2)11-20-16(19)14-10-7-6-9-13(14)15(17)18/h6-7,9-10,12H,3-5,8,11H2,1-2H3,(H,17,18)
DJDSLBVSSOQSLW-UHFFFAOYSA-N

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Applicazioni

Phthalic acid mono-2-ethylhexyl ester can be used as a precursor:
  • To synthesize dioctyl phthalate, a widely used plasticizer, via esterification reaction with 2-ethylhexanol.
  • To prepare a fluorescent probe, 2-[[(3′,6′-dihydroxy-3-oxospiro[isobenzofuran-1(3H),9′-[9H]xanthen]-5-yl)amino]carbonyl] 2-ethylhexyl benzoic acid ester, to detect toxic metabolite mono-2-ethylhexyl phthalate (MEHP).

Pittogrammi

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3


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Reactive Extraction Strategy for Synthesizing Dioctyl Phthalate Intensified by Bifunctional Deep Eutectic Solvent [Im: 2PTSA]
Qin Hao, et al.
Chemical Engineering and Processing, 157, 108060-108060 (2020)
Da-Hye Kim et al.
Molecules (Basel, Switzerland), 24(8) (2019-04-24)
Endocrine active compounds with structural similarities to natural hormones such as 17β-estradiol (E2) and androgen are suspected to affect the human endocrine system by inducing hormone-dependent effects. This study aimed to detect the (anti-)estrogenic and (anti-)androgenic activities of mono-(2-ethylhexyl) phthalate
Chunjiao Lu et al.
Ecotoxicology and environmental safety, 208, 111525-111525 (2020-10-30)
The base excision repair (BER) pathway is an important defense response to oxidative DNA damage. It is known that exposures to phthalate esters (PAEs), including Dibutyl phthalate (DBP), Mono-(2-ethylhexyl) phthalate (MEHP), and Di-(2-ethylhexyl) phthalate (DEHP), cause reactive oxygen species-induced DNA
Jijun Shang et al.
Toxicological sciences : an official journal of the Society of Toxicology, 168(1), 78-94 (2018-11-07)
Bisphenols and phthalates leach from medical devices, and this exposure is likely to increase in postcardiac surgery patients. Previous studies suggest that such chemical exposure may impact recovery and wound healing, yet the direct effects of bisphenols and phthalates are
Xiaoju Ma et al.
Toxicology research, 8(4), 522-530 (2019-08-02)
Recent reports have concentrated on some androgens/antiandrogens and confirmed that certain chemicals have demonstrated androgenic/antiandrogenic activities in vitro. However, it is still unknown whether more chemicals in the human environment possess endocrine toxicity. 58A novel AR-mediated reporter gene assay based

Global Trade Item Number

SKUGTIN
R251070-1EA
796832-500MG4061832964430

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