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HomeProduct name list2-Ethylhexyl 4-dimethylaminobenzoate

2-Ethylhexyl 4-dimethylaminobenzoate

Synonym(s):EHDAB;Octyl dimethyl PABA;2-Ethylhexyl 4-(dimethylamino)benzoate;4-(Dimethylamino)benzoic acid 2-ethylhexyl ester;2-Ethylhexyl N ,N -dimethyl-p -aminobenzoate

  • CAS NO.:21245-02-3
  • Empirical Formula: C17H27NO2
  • Molecular Weight: 277.4
  • MDL number: MFCD00017526
  • EINECS: 244-289-3
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-11-01 18:09:03
2-Ethylhexyl 4-dimethylaminobenzoate  Structural

What is 2-Ethylhexyl 4-dimethylaminobenzoate ?

Absorption

Padimate O is capable of human skin penetration .

Toxicity

Padimate O causes DNA strand breaks of cells under the epidermis in vitro . No LD50 value reported.

Chemical properties

Colorless to yellow liquid

The Uses of 2-Ethylhexyl 4-dimethylaminobenzoate

Ultraviolet screen Arlatone.

The Uses of 2-Ethylhexyl 4-dimethylaminobenzoate

padimate O is the drug name for ethylhexyl dimethyl PABA, a sunscreen chemical formerly known as octyl dimethyl PABA.

The Uses of 2-Ethylhexyl 4-dimethylaminobenzoate

2-ethylhexyl-4-dimethyl-amino-benzoate is used as an UV-B-absorbing agent in sunscreens and cosmetic creams, lotions, lipsticks, sun oils, moisturizers, nail polish, etc.

Background

Padimate O is an active sunscreen agent in cosmetics and over-the-counter sunscreen drug products in concentrations up to 8%, as regulated by the FDA . It is a structurally-related compound to Aminobenzoic acid that absorbs UV-B rays to prevent photodamage. It penetrates human skin, and is shown to induce non-ligatable strand breaks on DNA in vitro and mutagenic effects on yeast in vivo .

Indications

Indicated as an active UV-B filter to prevent photodamage.

Definition

ChEBI: Padimate O is a benzoate ester.

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.

Pharmacokinetics

Padimate O absorbs UV-B rays, which can in turn induce DNA damage in human keratinocytes. While treatment of padimate O suppresses the formation of UV-endonuclease-sensitive sites, there is also an increase in direct strand breaks of DNA in cells .

Metabolism

No pharmacokinetic data available.

Properties of 2-Ethylhexyl 4-dimethylaminobenzoate

Melting point: 242.5-243.5 °C
Boiling point: 325 °C (lit.)
Density  0.995 g/mL at 25 °C (lit.)
vapor pressure  0.001Pa at 25℃
refractive index  n20/D 1.542(lit.)
Flash point: >230 °F
storage temp.  Refrigerator
solubility  Chloroform (Slightly), Methanol (Slightly)
form  neat
pka 2.39±0.12(Predicted)
Specific Gravity 0.995
color  Off-White to Orange Waxy
Water Solubility  100μg/L at 20℃
Merck  14,3232
CAS DataBase Reference 21245-02-3(CAS DataBase Reference)
NIST Chemistry Reference Padimate o(21245-02-3)
EPA Substance Registry System 2-Ethylhexyl p-dimethylaminobenzoate (21245-02-3)

Safety information for 2-Ethylhexyl 4-dimethylaminobenzoate

Signal word Danger
Pictogram(s)
ghs
Health Hazard
GHS08
Precautionary Statement Codes P201:Obtain special instructions before use.
P202:Do not handle until all safety precautions have been read and understood.
P280:Wear protective gloves/protective clothing/eye protection/face protection.
P308+P313:IF exposed or concerned: Get medical advice/attention.
P405:Store locked up.
P501:Dispose of contents/container to..…

Computed Descriptors for 2-Ethylhexyl 4-dimethylaminobenzoate

InChIKey WYWZRNAHINYAEF-UHFFFAOYSA-N

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