Skip to Content
Merck
All Photos(1)

Documents

41774

Sigma-Aldrich

1,4-Dimethoxynaphthalene

for fluorescence, fluorescent marker, ≥99.5% (HPLC)

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C12H12O2
CAS Number:
Molecular Weight:
188.22
Beilstein:
2048082
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

grade

for fluorescence

Assay

≥99.5% (HPLC)

fluorescence

λex 318 nm; λem 394 nm in ethanol (1 mg/mL)

storage temp.

2-8°C

SMILES string

COc1ccc(OC)c2ccccc12

InChI

1S/C12H12O2/c1-13-11-7-8-12(14-2)10-6-4-3-5-9(10)11/h3-8H,1-2H3

InChI key

FWWRTYBQQDXLDD-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

1,4-Dimethoxynaphthalene may be used as a reference molecule during the synthesis, separation and analysis of derivatized naphthalenes.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

M Abdel-Mogib et al.
Die Pharmazie, 57(4), 286-287 (2002-05-10)
Chromatographic separation of an ethanolic extract of rhizomes of Asphodelus tenuifolius Cav. (Asphodelaceae) yielded in addition to beta-sitosterol, stigmasterol and two anthraquinone derivatives, 1,8-dimethoxynaphthalene as well as two new naphthalene derivatives. The new compounds were identified as 2-acetyl-8-methoxy-3-methyl-1-naphthol and 2-acetyl-1,8-dimethoxy-3-methylnaphthalene.
Samik Upadhaya et al.
Cell stem cell, 27(2), 336-345 (2020-06-27)
Adult mammalian hematopoietic stem cells (HSCs) reside in the bone marrow (BM) but can be mobilized into blood for use in transplantation. HSCs interact with BM niche cells that produce growth factor c-Kit ligand (Kitl/SCF) and chemokine CXCL12, and were
Cécile Pégurier et al.
Bioorganic & medicinal chemistry, 11(5), 789-800 (2003-01-23)
Amido derivatives 10-18 of the corresponding oxyamines were synthesised as melatoninergic ligands by the reaction of hydroxyphtalimide with the halogeno derivatives or the corresponding alcohols using Mitsunobu reaction conditions. The affinity of the compounds for chicken brain melatonin receptors and

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service