모든 사진(1)
About This Item
Linear Formula:
(HO)C6H4CO2CH2CH(C2H5)(CH2)3CH3
CAS Number:
Molecular Weight:
250.33
Beilstein:
2730664
EC Number:
MDL number:
UNSPSC 코드:
12162002
PubChem Substance ID:
NACRES:
NA.23
추천 제품
Quality Level
분석
99%
양식
liquid
refractive index
n20/D 1.502 (lit.)
bp
189-190 °C/21 mmHg (lit.)
density
1.014 g/mL at 25 °C (lit.)
SMILES string
CCCCC(CC)COC(=O)c1ccccc1O
InChI
1S/C15H22O3/c1-3-5-8-12(4-2)11-18-15(17)13-9-6-7-10-14(13)16/h6-7,9-10,12,16H,3-5,8,11H2,1-2H3
InChI key
FMRHJJZUHUTGKE-UHFFFAOYSA-N
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일반 설명
2-Ethylhexyl salicylate(EHS) is an organic ultraviolet(UV) absorber that can be used as a photostable ingredient in cosmetic formulations. It shows an absorption spectra in the range of 280-320 nm in the UV region.
애플리케이션
EHS is a salicylic ester which can be used as an UV filter in sunscreen based creams.
신호어
Warning
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Aquatic Chronic 1
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point (°F)
323.6 °F - closed cup
Flash Point (°C)
162 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
Lot/Batch Number
이미 열람한 고객
A pendant peptide endows a sunscreen with water-resistance.
Ellison AJ and Raines RT
Organic & Biomolecular Chemistry, 16(39), 7139-7142 (2018)
Optical and electron paramagnetic resonance studies of the excited triplet states of UV-B absorbers: 2-ethylhexyl salicylate and homomenthyl salicylate.
Sugiyama K, et al.
Photochemical & Photobiological Sciences : Official Journal of the European Photochemistry Association and the European Society for Photobiology, 14(9), 1651-1659 (2015)
M McVean et al.
Molecular carcinogenesis, 24(3), 169-176 (1999-04-16)
Topical application of alpha-tocopherol (alphaTH), the most prominent naturally occurring form of vitamin E, inhibits ultraviolet (UV) B-induced photocarcinogenesis and DNA photodamage in C3H mice in vivo. In this study, we compared alphaTH with other vitamin E compounds and with
M McVean et al.
Carcinogenesis, 18(8), 1617-1622 (1997-08-01)
Ultraviolet B (UVB, 290-320 nm) exposure results in a variety of cellular insults including induction of cyclobutane pyrimidine dimers in DNA. Accumulation of these lesions can lead to mutations in critical genes and contribute to the development of nonmelanoma skin
K A Walters et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 35(12), 1219-1225 (1998-02-04)
The human skin penetration of [14C]octyl salicylate from two representative sunscreen vehicles was determined in vitro. 3H-sucrose was incorporated into all formulations and provided a marker for membrane integrity. When applied as a finite dose in an oil-in-water emulsion vehicle
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