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Dipentyl phthalate

analytical standard

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About This Item

Formula empirica (notazione di Hill):
C18H26O4
Numero CAS:
Peso molecolare:
306.40
Beilstein:
1987323
Numero CE:
Numero MDL:
Codice UNSPSC:
12000000
ID PubChem:

Grado

analytical standard

CdA

current certificate can be downloaded

Confezionamento

ampule of 1000 mg

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Densità

1.025 g/mL at 20 °C (lit.)

applicazioni

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

Temperatura di conservazione

2-30°C

Stringa SMILE

CCCCCOC(=O)c1ccccc1C(=O)OCCCCC

InChI

1S/C18H26O4/c1-3-5-9-13-21-17(19)15-11-7-8-12-16(15)18(20)22-14-10-6-4-2/h7-8,11-12H,3-6,9-10,13-14H2,1-2H3
IPKKHRVROFYTEK-UHFFFAOYSA-N

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Descrizione generale

Dipentyl phthalate belongs to the group of phthalates, widely used as plasticizers in plastics and for consumer applications. It is a major contaminant and can be released from a variety of products into the environment.

Applicazioni

Dipentyl phthalate may be used as an analytical reference standard for the quantification of the analyte in water, juice and milk samples using high-performance liquid chromatography (HPLC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pittogrammi

Health hazardEnvironment

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Aquatic Acute 1 - Repr. 1B

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

244.4 °F - closed cup

Punto d’infiammabilità (°C)

118 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Certificati d'analisi (COA)

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Graphene reinforced hollow fiber liquid-phase microextraction for the determination of phthalates in water, juice and milk samples by HPLC
Sun M, et al.
Analytical Methods : Advancing Methods and Applications, 5(20), 5694-5700 (2013)
Ji-Young Ahn et al.
Current microbiology, 52(5), 340-344 (2006-04-06)
The efficiency of two lipolytic enzymes (fungal cutinase and yeast esterase) in the degradation of dipentyl phthalate (DPeP) was investigated. The DPeP degradation rate of fungal cutinase was surprisingly high, i.e., almost 60% of the initial DPeP (500 mg/L) was
J J Heindel et al.
Toxicology and applied pharmacology, 97(2), 377-385 (1989-02-01)
High doses of phthalate esters in vivo cause testicular lesions. One initial target for these effects is the sustentacular Sertoli cell. Sertoli cells are unique in that they have surface membrane receptors for follicle-stimulating hormone (FSH), which couple to adenylate
N P Moore et al.
Archives of toxicology, 66(6), 435-442 (1992-01-01)
Cell-specific testicular toxicants have been used to examine the distribution of creatine within the rat testis, and to examine the potential use of creatinuria as a non-invasive indicator of testicular damage. Groups of rats were administered single doses of various
D M Creasy et al.
Experimental and molecular pathology, 46(3), 357-371 (1987-06-01)
A sequential morphological study has been carried out to examine the ultrastructural effects of di-n-pentyl phthalate (DPP) on the mature rat testis. A single oral dose of 2.2 g DPP/kg body wt was administered, and testes, perfuse-fixed 3-48 hr after

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