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Merck
CN

79291

4-[2-(N,N-Dimethylamino)ethylaminosulfonyl]-7-(2-aminoethylamino)-2,1,3-benzoxadiazole

derivatization grade (HPLC), LiChropur, ≥95.0% (HPLC)

Synonym(s):

4-[2-(N,N-Dimethylamino)ethylsulfamoyl]-7-(2-aminoethylamino)benzofurazan, 7-[(2-Aminoethyl)amino]-N-[2-(dimethylamino)ethyl]-2,1,3-benzoxadiazole-4-sulfonamide, DAABD-AE

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About This Item

Empirical Formula (Hill Notation):
C12H20N6O3S
CAS Number:
Molecular Weight:
328.39
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
23151816
MDL number:
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grade

derivatization grade (HPLC)

Quality Segment

assay

≥95.0% (HPLC)

form

powder

quality

LiChropur

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable

storage temp.

2-8°C

SMILES string

CN(C)CCNS(=O)(=O)c1ccc(NCCN)c2nonc12

InChI

1S/C12H20N6O3S/c1-18(2)8-7-15-22(19,20)10-4-3-9(14-6-5-13)11-12(10)17-21-16-11/h3-4,14-15H,5-8,13H2,1-2H3

InChI key

QKTBJERNSIEPPM-UHFFFAOYSA-N

Application

4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-(2-aminoethylamino)-2,1,3-benzoxadiazole (DAABD-AE) is a new derivatization reagent for rapid and specific liquid chromatography tandem mass spectrometric quantification of pristanic acid, phytanic acid, and very long chain fatty acids (i.e., hexacosanoic, tetracosanoic, and docosanoic acids) in plasma.
4-[2-(N,N-Dimethylamino)ethylaminosulfonyl]-7-(2-aminoethylamino)-2,1,3-benzoxadiazole may be used as derivatization reagent for the trace analysis of carboxylic acids in saliva samples using liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS).

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

新产品

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Osama Y Al-Dirbashi et al.
Journal of lipid research, 49(8), 1855-1862 (2008-04-29)
Quantification of pristanic acid, phytanic acid, and very long chain fatty acids (i.e., hexacosanoic, tetracosanoic, and docosanoic acids) in plasma is the primary method for investigateing a multitude of peroxisomal disorders (PDs). Typically based on GC-MS, existing methods are time-consuming
Yuhki Tsukamoto et al.
Biomedical chromatography : BMC, 19(10), 802-808 (2005-06-15)
The derivatization regents for carboxylic acids, DAABD-AE (4-[2-(N,N-dimethylamino)ethylaminosulfonyl]7-(2-aminoethylamino)-2,1,3-benzoxadiazole), MePZBD-AE ([4-(4-N-methyl)piperazinosulfonyl]-7-(2-aminoethylamino)-2,1,3-benzoxadiazole) and APZBD-NHMe ([4-(4-N-aminoethyl)piperazinosulfonyl]-7-methylamino-2,1,3-benzoxadiazole) were developed for electrospray ionization-mass spectrometry (ESI-MS). The derivatization reaction with fatty acids was completed at 60 degrees C within 30 min. The derivatives of fatty acids
Milene Volpato et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 1055-1056, 125-134 (2017-05-04)
As pre-clinical and clinical research interest in ω-3 polyunsaturated fatty acids (PUFA) increases, so does the need for a fast, accurate and reproducible analytical method to measure fatty acids (FA) in biological samples in order to validate potential prognostic and



Global Trade Item Number

SKUGTIN
79291-100MG04061834410843