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2-Ethylhexyl 4-(dimethylamino)benzoate - 98%, high purity , CAS No.21245-02-3

  • ≥98%
Item Number
E102208
Grouped product items
SKUSizeAvailabilityPrice Qty
E102208-25ml
25ml
In stock
$36.90
E102208-100ml
100ml
In stock
$129.90
E102208-500ml
500ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$584.90

Basic Description

Synonyms2-Ethylhexyl 4-(dimethylamino)benzoate|21245-02-3|Padimate O|2-ETHYLHEXYL 4-DIMETHYLAMINOBENZOATE|Escalol 507|Padimate-O|Octyl dimethyl PABA|Arlatone UVB|Eusolex 6007|2-Ethylhexyl p-dimethylaminobenzoate|Benzoic acid, 4-(dimethylamino)-, 2-ethylhexyl este
Specifications & Purity≥98%
Shipped InNormal

Associated Targets

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NR3C1 Tclin Glucocorticoid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CBX1 Tbio Chromobox protein homolog 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RORC Tchem Nuclear receptor ROR-gamma 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HSD17B10 Tchem 3-hydroxyacyl-CoA dehydrogenase type-2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PIN1 Tchem Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PLK1 Tchem Serine/threonine-protein kinase PLK1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

LMNA Tbio Prelamin-A/C 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CLPP Tchem ATP-dependent Clp protease proteolytic subunit, mitochondrial 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALDH1A1 Tchem Retinal dehydrogenase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

THRB Tclin Thyroid hormone receptor beta 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KCNH2 Tclin Potassium voltage-gated channel subfamily H member 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CXCL8 Tchem Interleukin-8 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KDM4A Tchem Lysine-specific demethylase 4A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid488183116
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488183116
IUPAC Name 2-ethylhexyl 4-(dimethylamino)benzoate
INCHI 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
Canonical SMILES CCCCC(CC)COC(=O)C1=CC=C(C=C1)N(C)C
Isomeric SMILES CCCCC(CC)COC(=O)C1=CC=C(C=C1)N(C)C
WGK Germany 2
PubChem CID 30541
Molecular Weight 277.4
Reaxy-Rn 5946517

Certificates

Certificate of Analysis(COA)

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To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

6 results found

Lot NumberCertificate TypeDateItem
J1211051Certificate of AnalysisJul 16, 2024 E102208
G2307600Certificate of AnalysisJul 15, 2023 E102208
C1911198Certificate of AnalysisJan 11, 2023 E102208
F2221216Certificate of AnalysisJun 07, 2022 E102208
F2221512Certificate of AnalysisJun 07, 2022 E102208
D2310285Certificate of AnalysisDec 15, 2021 E102208

Chemical and Physical Properties

SolubilityInsoluble in water; Soluble in Alcohol; Slightly soluble in Ether
SensitivityAir Sensitive
Refractive Index1.542
Flash Point(°F)113 °C
Flash Point(°C)113°C
Boil Point(°C)325°C

Safety and Hazards(GHS)

Pictogram(s) GHS07
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

WGK Germany 2
Reaxy-Rn 5946517
Merck Index 3232

Related Documents

References

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