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4-tert-Octylphenol monoethoxylate solution

1 μg/mL in acetone, analytical standard

Synonyme(s) :

2-[4-(1,1,3,3-Tetramethylbutyl)phenoxy]ethanol

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About This Item

Formule empirique (notation de Hill):
C16H26O2
Numéro CAS:
2315-67-5
Poids moléculaire :
250.38
Numéro Beilstein :
2114647
Numéro CE :
200-662-2
Numéro MDL:
MFCD00214058
Code UNSPSC :
41116107
ID de substance PubChem :
329754376
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Durée de conservation

limited shelf life, expiry date on the label

Concentration

1 μg/mL in acetone

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

environmental

Format

single component solution

Température de stockage

−20°C

Chaîne SMILES 

CC(C)(C)CC(C)(C)c1ccc(OCCO)cc1

InChI

1S/C16H26O2/c1-15(2,3)12-16(4,5)13-6-8-14(9-7-13)18-11-10-17/h6-9,17H,10-12H2,1-5H3

Clé InChI

JYCQQPHGFMYQCF-UHFFFAOYSA-N

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Description générale

Sigma-Aldrich offers 4-tert-octylphenol (1 μg/mL in acetone) monoethoxylate solution for a variety of applications that include, but are not limited to, environmental, food and beverage, forensics, petrochemical and pharmaceutical analyzes.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogrammes

FlameExclamation mark
GHS02,GHS07

Mention d'avertissement

Danger

Mentions de danger

H225,H319,H336

Conseils de prudence

P210 - P305 + P351 + P338

Classification des risques

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Organes cibles

Central nervous system

Risques supp

EUH066

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

1.4 °F - closed cup

Point d'éclair (°C)

-17 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves

Choose from one of the most recent versions:

Certificats d'analyse (COA)

Lot/Batch Number
BCCB3617
BCBW3021
BCBT6285
SZBC115XV
SZE9294X

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Olga Pougovkina et al.
Human molecular genetics, 23(13), 3513-3522 (2014-02-12)
Mitochondria integrate metabolic networks for maintaining bioenergetic requirements. Deregulation of mitochondrial metabolic networks can lead to mitochondrial dysfunction, which is a common hallmark of many diseases. Reversible post-translational protein acetylation modifications are emerging as critical regulators of mitochondrial function and
Marie Orre et al.
Neurobiology of aging, 35(12), 2746-2760 (2014-07-09)
Reactive astrocytes and microglia are associated with amyloid plaques in Alzheimer's disease (AD). Yet, not much is known about the molecular alterations underlying this reactive phenotype. To get an insight into the molecular changes underlying AD induced astrocyte and microglia
Nobuhiko Hamazaki et al.
Development (Cambridge, England), 142(5), 910-920 (2015-01-31)
In mice, zygotic activation occurs for a wide variety of genes, mainly at the 2-cell stage. Long noncoding RNAs (lncRNAs) are increasingly being recognized as modulators of gene expression. In this study, directional RNA-seq of MII oocytes and 2-cell embryos
Pasqualino De Antonellis et al.
Molecular & cellular proteomics : MCP, 13(8), 2114-2131 (2014-06-11)
Several genes encoding for proteins involved in proliferation, invasion, and apoptosis are known to be direct miR-34a targets. Here, we used proteomics to screen for targets of miR-34a in neuroblastoma (NBL), a childhood cancer that originates from precursor cells of
Matasha Dhar et al.
Molecular endocrinology (Baltimore, Md.), 28(7), 1073-1087 (2014-06-01)
Leptin acts in the hippocampus to enhance cognition and reduce depression and anxiety. Cognitive and emotional disorders are associated with abnormal hippocampal dendritic spine formation and synaptogenesis. Although leptin has been shown to induce synaptogenesis in the hypothalamus, its effects
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