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Key Documents

H17309

Sigma-Aldrich

Hydrindantin

≥97%

Synonym(s):

2,2′-Dihydroxy-2,2′-biindan-1,1′,3,3′-tetrone

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About This Item

Empirical Formula (Hill Notation):
C18H10O6
CAS Number:
Molecular Weight:
322.27
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥97%

mp

252 °C (dec.) (lit.)

SMILES string

OC1(C(=O)c2ccccc2C1=O)C3(O)C(=O)c4ccccc4C3=O

InChI

1S/C18H10O6/c19-13-9-5-1-2-6-10(9)14(20)17(13,23)18(24)15(21)11-7-3-4-8-12(11)16(18)22/h1-8,23-24H

InChI key

LWFPYLZOVOCBPZ-UHFFFAOYSA-N

Application

Used in the determination of amino acids.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Soft matter, 15(2), 303-311 (2018-12-18)
Nano-clays (NCs) as a representative type of nano-materials are a source of inspiration for design of new biomedical materials with excellent performances. Research has shown that guanidinium ions (Gu+) can form non-covalent salt-bridge interactions with NCs, serving as "molecular glue"
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Carbohydrate polymers, 203, 302-309 (2018-10-16)
The malignant gliomas are most destructive brain tumor having low drug response. The thermosensitive hydrogel from pluronic F127 (PF127) and N,N,N-trimethyl chitosan (TMC) is developed as a drug delivery system for anticancer drug docetaxel (DTX) to the glioblastoma multiforme. The
Shi Cheng et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 1159, 122402-122402 (2020-11-02)
An affinity ligand was designed from 1-aminocyclohexane based on the crystal structure of Streptomyces albidoflavus phospholipase A1 (saPLA1) by using Discovery Studio software. The molecular docking results indicated that the designed ligand could interact with the active pocket of saPLA1.
Yihua Pei et al.
Journal of controlled release : official journal of the Controlled Release Society, 267, 133-143 (2017-08-12)
Methicillin-resistant Staphylococcus aureus (MRSA) infection is a serious threat to the public health. MRSA is particularly difficult to treat when it invades host cells and survive inside the cells. Although vancomycin is active against MRSA, it does not effectively kill

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