10401-59-9

Basic information

• Product Name: 9-ANTHRYLDIAZOMETHANE
• Synonyms: ADAM;9-ANTHRYLDIAZOMETHANE;9-(DIAZOMETHYL)ANTHRACENE;ADAM 9-Anthryldiazomethane;Anthryldiazomethane;9-(Diazomethyl)anthracene, ADAM;Anthracene-9-yldiazomethane
• CAS NO: 10401-59-9
• Molecular Formula: C₁₅H₁₀N₂
• Molecular Weight: 218.25
• Mol File: 10401-59-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 65-67 °C
• Appearance: /
• Storage Temp.: −20°C
• CAS DataBase Reference: 9-ANTHRYLDIAZOMETHANE(CAS DataBase Reference)
• NIST Chemistry Reference: 9-ANTHRYLDIAZOMETHANE(10401-59-9)
• EPA Substance Registry System: 9-ANTHRYLDIAZOMETHANE(10401-59-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 10401-59-9(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 10401-59-9 differently. You can refer to the following data:
1. Fluorescent probe for direct carboxylic acid modification.
2. 9-Anthryldiazomethane (ADAM) is a fluorescent diazomethane analog used to identify bile acids, amino acids, fatty acids, steroid acids, and prostaglandins. In addition, derivatives of 9-Anthryldiazomethane can be detected using liquid chromatography-mass spectrometry. Furthermore, the fluorescence of these analogs can be detected at 254nm and 412 nm. Alternate studies indicate that 9-Anthryldiazomethane can be used to identify prostaglandins in plasma assays using HPLC.

InChI:InChI=1/C15H10N2/c16-17-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-10H

Upstream product

• 7512-18-7 anthracen-9-ylmethylene-hydrazone 

Downstream Products

• 38418-19-8 Benzoesaeure(anthr-9-ylmethylester) 
• 157606-35-4 okadaic acid 9-anthrylmethylester 
• 16430-34-5 9-(phenoxymethyl)anthracene 

Related news

Phorbol myristate acetate-stimulated release of cyclooxygenase products in rat pleural cells: Derivatization of prostaglandins with 9-ANTHRYLDIAZOMETHANE (cas 10401-59-9) for fluorometric determination by high performance liquid chromatography08/05/2019

White cells were collected from the wash of rat pleural cavity after exsanguination. The incubation mixture of the pleural cells with 1 μM phorbol myristate acetate (PMA) was extracted with acidified ethanol and purified with a Sep-pak C18. The resultant fraction containing prostaglandins (PG) ...detailed

Assessment of fatty acids in cardiac tissue as 9-ANTHRYLDIAZOMETHANE (cas 10401-59-9) esters by high-performance liquid chromatography08/02/2019

A high-performance liquid chromatographic technique for the rapid assessment of fatty acids in cardiac tissue is described. A level of 50.4 ± 14.9 nmol fatty acids per g wet weight of rat myocardial tissue could be monitored. The content of the individual fatty acids C14:0, C16:0, C16:1, C18:0,...detailed

Improved method for preparation and use of 9-ANTHRYLDIAZOMETHANE (cas 10401-59-9) for derivatization of hydroxycarboxylic acids08/01/2019

Application of a method for the “in situ” generation of 9-anthryldiazomethane (ADAM) to the derivatization of the carboxyl function in diarrhetic shellfish poisoning (DSP) toxins revealed the formation of artifact products. Using liquid chromatography–mass spectrometry, it was determined that...detailed

New preparation method for 9-ANTHRYLDIAZOMETHANE (cas 10401-59-9) (ADAM) as a fluorescent labeling reagent for fatty acids and derivatives07/30/2019

A preparation method for 9-anthryldiazomethane (ADAM) as a fluorescent labeling reagent for carboxylic acids is described. 9-Anthraldehyde hydrazone is oxidized with an organic oxidant, N-chlorosuccinimide, in an organic solvent such as ethyl acetate to give ADAM, and then the reaction mixture i...detailed

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