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389439

1-Pyrenemethanol

Name: 1-Pyrenemethanol
Brand: ALDRICH

98%

Synonym(s):

1-(1-Hydroxymethyl)pyrene, 1-Hydroxymethylpyrene

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About This Item

Empirical Formula (Hill Notation):

C₁₇H₁₂O

CAS Number:

24463-15-8

Molecular Weight:

232.28

NACRES:

NA.22

PubChem Substance ID:

24864285

UNSPSC Code:

12352100

MDL number:

MFCD00029252

Assay:

98%

Form:

solid

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Properties

Quality Level

100

assay

98%

form

solid

mp

123-126 °C (lit.)

functional group

hydroxyl

SMILES string

OCc1ccc2ccc3cccc4ccc1c2c34

InChI

1S/C17H12O/c18-10-14-7-6-13-5-4-11-2-1-3-12-8-9-15(14)17(13)16(11)12/h1-9,18H,10H2

InChI key

NGDMLQSGYUCLDC-UHFFFAOYSA-N

Description

Application

1-Pyrenemethanol can be used:

For the synthesis of pincer-like benzene-bridged fluorescent selective sensor for adenosine-5′-triphosphate (ATP) detection.
As a starting material for the synthesis of pyrene-end poly(glycidyl methacrylate) polymer.
As an initiator for the synthesis of pyrene core star polymers.
For the synthesis of 1-pyrenecarboxaldehyde, an important intermediate in pharmaceutical and agrochemical fields.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Development of hydroxysteroid sulfotransferase-deficient lesions during hepatocarcinogenesis in rats.

G Werle-Schneider et al.

Carcinogenesis, 14(11), 2267-2270 (1993-11-01)

Rat liver cytosolic hydroxysteroid sulfotransferases form highly reactive sulfuric acid esters from some benzylic alcohols, such as 1-hydroxymethylpyrene. In this study we examined the expression of hydroxysteroid sulfotransferase a (STa) in carcinogen-induced enzyme-altered, presumably preneoplastic, rat liver foci. Female Wistar

Quantitative analysis of multiple phenotype enzyme-altered foci in rat hepatocarcinogenesis experiments: the multipath/multistage model.

C D Sherman et al.

Carcinogenesis, 16(10), 2499-2506 (1995-10-01)

The promotional effect of phenobarbital and 1-hydroxymethyl-pyren on enzyme altered lesions in the rat liver were quantified within the framework of two separate multipath/multistage models. The experiment analyzed followed an initiation-promotion protocol in which female Wistar rats were initiated with

Sulfotransferase-mediated chlorination of 1-hydroxymethylpyrene to a mutagen capable of penetrating indicator cells.

H Glatt et al.

Environmental health perspectives, 88, 43-48 (1990-08-01)

Methylated polycyclic aromatic hydrocarbons are common in the human environment. Many of them are stronger carcinogens than their purely aromatic congeners. They may be metabolized to benzylic alcohols. We report here on biochemical and toxicological characteristics of 1-hydroxymethylpyrene (HMP), a

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Global Trade Item Number

SKU	GTIN
389439-10G	04061831970791
389439-1G	04061831970852