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Merck
CN

80028

Chrysoidine G

analytical standard

Synonym(s):

4-Phenylazo-m-phenylenediamine monohydrochloride, Basic Orange 2, Chrysoidine Y

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About This Item

Empirical Formula (Hill Notation):
C12H12N4 · HCl
CAS Number:
Molecular Weight:
248.71
EC Number:
208-545-8
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Colour Index Number:
11270
Beilstein/REAXYS Number:
3724653
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InChI

1S/C12H12N4.ClH/c13-9-6-7-12(11(14)8-9)16-15-10-4-2-1-3-5-10;/h1-8H,13-14H2;1H

SMILES string

Cl[H].Nc1ccc(N=Nc2ccccc2)c(N)c1

InChI key

MCTQNEBFZMBRSQ-UHFFFAOYSA-N

grade

analytical standard

assay

≥95.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

mp

235 °C (dec.) (lit.)

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

neat

storage temp.

2-8°C

Quality Level

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Muta. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


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Rhiannon M David et al.
Environmental toxicology and chemistry, 28(9), 1893-1900 (2009-04-24)
The use of unicellular algae in ecotoxicity testing is well established, particularly regarding whole-organism and population-level end points such as lethality and population growth. Conflicting information exists, however, on the potential for genetic toxicity to be incorporated into the safety
Maggots dyed with chrysoidine.
British medical journal (Clinical research ed.), 289(6456), 1451-1452 (1984-11-24)
P Sandhu et al.
Toxicology letters, 58(1), 43-50 (1991-09-01)
Rat liver postmitochondrial supernatant (S9) converted the azo dyes chrysoidine Y and R to products that were mutagenic towards Salmonella typhimurium strain TA100. No such release of mutagens was demonstrated using intact rat hepatocytes as an activation system despite the
Ardeshir Shokrollahi et al.
Journal of hazardous materials, 160(2-3), 435-440 (2008-04-25)
A cloud point extraction procedure was presented for the preconcentration of copper(II) ion in various samples. After complexation by 4-(phenyl diazenyl) benzene-1,3-diamine (PDBDM) (chrysoidine), copper(II) ions were quantitatively recovered in Triton X-114 after centrifugation. 0.5ml of methanol acidified with 1.0molL(-1)
G Sole et al.
Lancet (London, England), 1(8444), 1477-1479 (1985-06-29)
In a case-control study of 240 men with urothelial cancer diagnosed in 1984 and 240 matched control subjects smoking and coarse fishing were found to be significantly associated with the disease. Duration of exposure to the chrysoidine azo dyes used

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