ChemicalBook--->CAS DataBase List--->88235-25-0

88235-25-0

88235-25-0 Structure

88235-25-0 Structure
IdentificationBack Directory
[Name]

6-(7-NITRO-2,1,3-BENZOXADIAZOL-4-YLAMINO)HEXANOIC ACID
[CAS]

88235-25-0
[Synonyms]

N316
NBD-X
C6-NBD
NBD-X acid
NBD Hexanoic Acid
7-nitrobenzoxadiazole-6-aminohexanoic acid
6-(7-NITROBENZOFURAZAN-4-YLAMINO)HEXANOIC ACID
6-(7-Nitrobenzofurazan-4-ylamino)hexano1c acid
6-(7-NITROBENZOFURAZAN-4-YLAMINO)- HEXANOIC ACID 97+%
6-(7-NITRO-2,1,3-BENZOXADIAZOL-4-YLAMINO)HEXANOIC ACID
6-[(4-nitro-2,1,3-benzoxadiazol-7-yl)amino]hexanoic acid
6-(N-(7-NITROBENZ-2-OXA-1,3-DIAZOL-4-YL)AMINO)HEXANOIC ACID
Hexanoic acid, 6-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]-
6-((7-Nitrobenzo[c][1,2,5]oxadiazol-4-yl)aMino)hexanoic acid
NBD-X [6-(N-(7-Nitrobenze-2-oxa-1,3-diazol-4-yl)aMino)hexanoic acid
[Molecular Formula]

C12H14N4O5
[MDL Number]

MFCD00057884
[MOL File]

88235-25-0.mol
[Molecular Weight]

294.26
Chemical PropertiesBack Directory
[Melting point ]

152 - 154°C
[Boiling point ]

559.4±60.0 °C(Predicted)
[density ]

1.462
[storage temp. ]

2-8°C(protect from light)
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

4.74±0.10(Predicted)
[color ]

Very Dark Orange
[BRN ]

6936249
[InChIKey]

DJFNQJJTTPMBIL-UHFFFAOYSA-N
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

23/24/25-36/37/38
[Safety Statements ]

22-26-36-45
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

3
[F ]

8
Hazard InformationBack Directory
[Uses]

6-(7-NITRO-2,1,3-BENZOXADIAZOL-4-YLAMINO)HEXANOIC ACID is used as a fluorescent probes for studying the fat globule (membrane) of bovine and human.
[Uses]

6-(7-NITRO-2,1,3-BENZOXADIAZOL-4-YLAMINO)HEXANOIC ACID is used for investigation of binding sites of fatty acid and sterol carrier proteins, also used for cell membrane staining.
[Uses]

NBD Hexanoic Acid is used as a fluorescent probes for studying the fat globule (membrane) of bovine and human.
[Definition]

ChEBI: A benzoxadiazole that is 2,1,3-benzoxadiazole which is substituted at positions 4 and 7 by (5-carboxypentyl)amino and nitro groups, respectively.
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