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74309

Supelco

Padimate O

analytical standard

Synonym(s):

2-Ethylhexyl 4-(dimethylamino)benzoate

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About This Item

Linear Formula:
(CH3)2NC6H4CO2CH2CH(C2H5)(CH2)3CH3
CAS Number:
Molecular Weight:
277.40
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.541±0.001
n20/D 1.542 (lit.)

bp

325 °C (lit.)

density

0.995 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

CCCCC(CC)COC(=O)c1ccc(cc1)N(C)C

InChI

1S/C17H27NO2/c1-5-7-8-14(6-2)13-20-17(19)15-9-11-16(12-10-15)18(3)4/h9-12,14H,5-8,13H2,1-4H3

InChI key

WYWZRNAHINYAEF-UHFFFAOYSA-N

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General description

Padimate O is a tertiary amine derivative of p-aminobenzoic acid (PABA), which is commonly used as a sunscreen agent in cosmetics and other sunscreen formulations due to its ability to absorb ultraviolet radiations.[1][2]

Application

Padimate O may be used as a reference standard in the determination of padimate O in cosmetics using high performance liquid chromatography (HPLC).[2]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Repr. 1B

Storage Class

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

wgk_germany

WGK 2

flash_point_f

374.0 °F - closed cup

flash_point_c

190 °C - closed cup


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Assay of mixtures of padimate-O and oxybenzone in sunscreen formulations by high-performance liquid chromatography.
Tan ISH, et al.
Journal of Chromatography A, 291, 275-282 (1984)
In vitro skin absorption and metabolism of Padimate-O and a nitrosamine formed in Padimate-O-containing cosmetic products.
Kenney EG, et al.
Journal of Society of Cosmetic Chemists of Japan, 46(2), 117-117 (1995)
Zacarías León-González et al.
Journal of chromatography. A, 1218(20), 3013-3021 (2011-04-13)
The in vivo metabolism of the xenobiotic agent 2-ethylhexyl 4-(N,N-dimethylamino)benzoate (EDP), a UV filter commonly used in sunscreen cosmetic products, was studied by targeting metabolomics analysis in human urine. The metabolomic study involved the use of urine from male and
T M Morgan et al.
Journal of pharmaceutical sciences, 87(10), 1226-1228 (1998-10-06)
The objective of this study was to determine if a novel metered-dose topical aerosol (MDTA) formulation containing the new dermal penetration enhancer, padimate O, could enhance the transdermal delivery of estradiol to an extent that would result in clinically relevant
Gamal M M El Maghraby et al.
International journal of pharmaceutics, 305(1-2), 90-104 (2005-10-04)
Employing thermal analysis, we investigated the mechanism of action of novel enhancers and probed phospholipid (PL) versus stratum corneum lipid (SCL) liposomes as model membranes. The enhancers included octyl salicylate (OS), padimate O (PADO) and 2-(1-nonyl)-1,3-dioxolane (ND). The negative controls

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