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Key Documents

54600

Sigma-Aldrich

4-Hydroxybenzhydrazide

suitable for fluorescence, ≥97.0% (T)

Synonym(s):

4-Hydroxybenzoic hydrazide, 4-Hydroxybenzoylhydrazine, p-Hydroxybenzoic acid hydrazide

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About This Item

Linear Formula:
HOC6H4CONHNH2
CAS Number:
Molecular Weight:
152.15
Beilstein/REAXYS Number:
473052
EC Number:
MDL number:
UNSPSC Code:
12352204
PubChem Substance ID:

assay

≥97.0% (T)

form

solid

mp

264-266 °C (dec.) (lit.)

fluorescence

λex 360 nm; λem 425 nm (after reaction with 5-hydroxymethyl-2-furaldehydezinc acetate)

suitability

suitable for fluorescence

SMILES string

NNC(=O)c1ccc(O)cc1

InChI

1S/C7H8N2O2/c8-9-7(11)5-1-3-6(10)4-2-5/h1-4,10H,8H2,(H,9,11)

InChI key

ZMZGIVVRBMFZSG-UHFFFAOYSA-N

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Other Notes

Reagent for the rapid automated determination of serum glucose[1]

replaced by

Product No.
Description
Pricing

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Automated method for serum glucose with p-hydroxybenzoic acid hydrazide.
B Fingerhut
Clinical chemistry, 19(9), 1022-1026 (1973-09-01)
A Jerlich et al.
Biochimica et biophysica acta, 1481(1), 109-118 (2000-09-27)
In this study, the production of the highly toxic oxidant hypochlorous acid (HOCl) by the phagocytic enzyme myeloperoxidase (MPO) was quantitated and the concomitant alterations of low density lipoprotein (LDL) were analyzed in view of the potential role of LDL
Andrea Mellitzer et al.
Biotechnology journal, 7(1), 155-162 (2011-05-04)
The exploitation of renewable resources for the production of biofuels relies on efficient processes for the enzymatic hydrolysis of lignocellulosic materials. The development of enzymes and strains for these processes requires reliable and fast activity-based screening assays. Additionally, these assays
Martin J Baumann et al.
Analytical biochemistry, 410(1), 19-26 (2010-11-16)
In lignocellulosic raw materials for biomass conversion, hemicelluloses constitute a substantial fraction, with xylan being the primary part. Although many pretreatments reduce the amount or change the distribution of xylan, it is important to degrade residual xylan so as to
Hanbin Xu et al.
International journal of biological macromolecules, 145, 527-534 (2019-12-25)
The interaction of polyphenolic catechins from Camellia sinensis tea with α-amylase, and the effects of the interactions on the kinetics of starch amylolysis, were investigated. Binding studies using surface plasmon resonance (SPR) and enzyme kinetic analysis indicated that the in

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