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17403

2,3-Dihydroxy-biphenyl

derivatization grade (GC derivatization), LiChropur™, ≥98.0%

Synonym(s):

2,3-Biphenyldiol, 3-Phenylpyrocatechol

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About This Item

Empirical Formula (Hill Notation):
C12H10O2
CAS Number:
1133-63-7
Molecular Weight:
186.21
PubChem Substance ID:
329751537
UNSPSC Code:
41116105
Beilstein/REAXYS Number:
1869593
MDL number:
MFCD00155166
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grade

derivatization grade (GC derivatization)

Quality Level

100

assay

≥98.0% (HPLC), ≥98.0%

form

solid

quality

LiChropur™

reaction suitability

reagent type: derivatization reagent
reaction type: Alkylations

technique(s)

gas chromatography (GC): suitable

mp

108-113 °C

SMILES string

Oc1cccc(-c2ccccc2)c1O

InChI

1S/C12H10O2/c13-11-8-4-7-10(12(11)14)9-5-2-1-3-6-9/h1-8,13-14H

InChI key

YKOQAAJBYBTSBS-UHFFFAOYSA-N

General description

Derivatization before a GC analysis helps in yielding distinctive products, which can be achieved using a derivatizing reagent that reacts with amino and hydroxyl functionalities quantitatively. 2,3-Dihydroxy-biphenyl (2,3-DHBP) is a derivatizing reagent.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
063681/1

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Sou Iijima et al.
Journal of bioscience and bioengineering, 109(6), 645-651 (2010-05-18)
A new method for isolating targeted live bacterial cells was established with the use of cell sorting by flow cytometry (FCM) based on the fluorescence of the intermediate metabolite of biphenyl degradation. During biphenyl degradation, a PCB degrader, Comamonas testosteroni
Ang Li et al.
Journal of environmental sciences (China), 21(2), 211-217 (2009-05-01)
A novel biphenyl-degrading bacterial strain LA-4 was isolated from activated sludge. It was identified as Dyella ginsengisoli according to phylogenetic similarity of 16S rRNA gene sequence. This isolate could utilize biphenyl as sole source of carbon and energy, which degraded
Min Gou et al.
Biotechnology letters, 34(1), 117-123 (2011-09-08)
A 2,3-dihydroxybiphenyl-1,2-dioxygenase gene (designated as bphC_meta) was identified in activated sludge metagenome by PCR. This gene shared 99% sequence identity with BphC from Burkholderia xenovorans LB400. The enzyme was purified from recombinant Escherichia coli with a subunit molecular mass of
Beatriz Cámara et al.
Environmental microbiology, 6(8), 842-850 (2004-07-15)
The degradation of polychlorobiphenyls (PCBs) by diverse bacteria, including Burkholderia sp. LB400, is incomplete with a concomitant accumulation of metabolic intermediates. In this study, the toxicity of diverse (chloro)biphenyls and of their biotransformation into the first two metabolic intermediates of
Shujuan Wang et al.
Analytical and bioanalytical chemistry, 410(27), 7145-7152 (2018-09-02)
In this work, we report a zeolitic imidazolate framework (ZIF-67) which could catalyze 3,3',5,5'-tetramethylbenzidine (TMB) to produce a yellow chromogenic reaction. ZIF-67 showed high peroxidase-like activity compared with copper-based metal-organic framework nanoparticles (Cu-MOF), zinc-based metal-organic framework nanoparticles (ZIF-8), and horseradish
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Global Trade Item Number

SKUGTIN
17403-100MG04061833276884

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