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Merck
CN

93524

4-(1-甲基肼基)-7-硝基苯并呋咱

derivatization grade (HPLC), LiChropur, ≥97.0%

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经验公式(希尔记法):
C7H7N5O3
化学文摘社编号:
分子量:
209.16
UNSPSC Code:
23151816
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
8316412
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InChI

1S/C7H7N5O3/c1-11(8)4-2-3-5(12(13)14)7-6(4)9-15-10-7/h2-3H,8H2,1H3

SMILES string

CN(N)c1ccc([N+]([O-])=O)c2nonc12

InChI key

GVUXVETWVIWDEV-UHFFFAOYSA-N

grade

derivatization grade (HPLC)

assay

≥97.0% (HPLC), ≥97.0%

form

powder

quality

LiChropur

technique(s)

HPLC: suitable

mp

~160 °C

storage temp.

2-8°C

Quality Level

Other Notes

Discover LiChropur reagents ideal for HPLC or LC-MS analysis
Superior reagent for monitoring aldehydes and ketones in air; Fluorogenic peroxidase substrate

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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4-(N-Methylhydrazino)-7-nitro-2,1,3-benzooxadiazole (MNBDH): A Novel Fluorogenic Peroxidase Substrate The authors would like to thank the Fonds der Chemischen Industrie (Frankfurt/Main) for financial support.
Meyer et al.
Angewandte Chemie (International ed. in English), 39(8), 1453-1455 (2000-04-25)
A Büldt et al.
Analytical chemistry, 71(9), 1893-1898 (1999-05-01)
The synthesis of N-methyl-4-hydrazino-7-nitrobenzofurazan (MNBDH) and its application as a new reagent for the determination of aldehydes and ketones are described. MNBDH reacts with carbonyl compounds in acidic media to the corresponding MNBD-hydrazones. In contrast to the established reagent 2,4-dinitrophenylhydrazine
A Büldt et al.
Analytical chemistry, 71(15), 3003-3007 (1999-08-18)
A selective and versatile fluorescence spectroscopic method for the determination of nitrite in waters has been developed. Nitrite reacts in the presence of mineral acids with the nonfluorescent N-methyl-4-hydrazino-7-nitrobenzofurazan forming N-methyl-4-amino-7-nitrobenzofurazan, which can be detected by fluorescence spectroscopy with an

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