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522546

Sigma-Aldrich

1,8-Dihydroxy-4,5-dinitroanthraquinone

97%

Synonym(s):

ARDP0006

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About This Item

Empirical Formula (Hill Notation):
C14H6N2O8
CAS Number:
81-55-0
Molecular Weight:
330.21
EC Number:
201-360-3
MDL number:
MFCD00019149
UNSPSC Code:
12352100
PubChem Substance ID:
24874279
NACRES:
NA.22

Assay

97%

mp

225 °C (dec.) (lit.)

SMILES string

Oc1ccc(c2C(=O)c3c(ccc(O)c3C(=O)c12)[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C14H6N2O8/c17-7-3-1-5(15(21)22)9-11(7)14(20)12-8(18)4-2-6(16(23)24)10(12)13(9)19/h1-4,17-18H

InChI key

GJCHQJDEYFYWER-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
01730JU

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David A Constant et al.
Proceedings of the National Academy of Sciences of the United States of America, 115(40), 10136-10141 (2018-09-20)
Many positive-strand RNA viruses translate their genomes as single polyproteins that are processed by host and viral proteinases to generate all viral protein products. Among these is dengue virus, which encodes the serine proteinase NS2B/3 responsible for seven different cleavages
Measurement and Correlation of Derivatized Anthraquinone Solubility in Supercritical Carbon Dioxide.
Alwi RS and Tamura K.
Journal of Chemical and Engineering Data, 60(10), 3046-3052 (2015)
Catalysed hydrogenation of hydroxynitroanthraquinones in strong acid.
Morley JO and Hutcheson R.
Journal of Chemical Technology and Biotechnology, 30(1), 409-414 (1980)

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