C.I. Solvent Red 80

HCID 22830CAS 6358-53-8

Grundinformationen

Standard-SMILES
COc1ccc(OC)c(N=Nc2c(O)ccc3ccccc23)c1
InChIKey
GJUABKCEXOMRPQ-UHFFFAOYSA-N
Summenformel
C18H16N2O3
Durchschnittliche Molmasse
308,3 g/mol
Monoisotopische Masse
308,11609237

Überblick

Citrus Red No. 2 can cause cancer according to California Labor Code.

Namen und Bezeichner

Bevorzugter Name
C.I. Solvent Red 80
IUPAC
1-[(2,5-dimethoxyphenyl)diazenyl]naphthalen-2-ol
Englischer Name
1-[(2,5-dimethoxyphenyl)azo]-2-naphthol
Summenformel
C18H16N2O3
Molmasse
308.33

Namen und Synonyme

6358-53-8C.I. Solvent Red 80DTXSID6024838DTXCID10809925RefChem:1080572CITRUS RED 2Solvent red 801-((2,5-Dimethoxyphenyl)diazenyl)naphthalen-2-olCitrus RedCitrus Red No. 21-[(2,5-dimethoxyphenyl)azo]-2-naphthol1-(2,5-Dimethoxyphenylazo)-2-naphthol
Weitere Namen anzeigen
C.I.12156CITRUSREDCITRUSRED2CITRUSREDNO.2Solvent Red 80.ditrus red 2-D6C.I.Solvent Red 80Blueberry red pigmentC.I.Solvent Red 80:C.I.12156Citrus Red 2 in Acetonitrile
CI Solvent Red 80Cerven rozpoustedlova 801-(2,5-Dimethyloxyphenylazo)-2-naphthol1-[(2,5-dimethoxyphenyl)diazenyl]naphthalen-2-ol2,5-Dimethoxy-1-(phenylazo)-2-naphtholC.I. 121561-(1-(2,5-Dimethoxyphenyl)azo)-2-naphthol2,5-Dimethoxybenzeneazo-beta-naphthol

Datenbank-Bezeichner

CAS
6358-53-8
PubChem CID
22830
DTXSID
DTXSID6024838
ChEMBL
CHEMBL3560990
ChEBI
CHEBI:82306
UNII
2QE5Y68984
EC Number
228-778-9
Nikkaji
J34.109F

Eigenschaften

Berechnete Struktureigenschaften

XLogP
4,5
Polarare Oberfläche (TPSA)
63,4 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
5
Frei drehbare Bindungen
4
Schwere Atome
23

Experimentelle und physikochemische Eigenschaften

Chemical Classes · 2 Einträge

Dyes -> Azo Dyes

Carcinogens

Food Additives · 2 Einträge

Foods -> FDA Regulatory Status of Color Additives

COLOR OR COLORING ADJUNCT -> FDA Substance added to food

Color/Form · 2 Einträge

Orange to yellow solid or dark red powder (NTP, 1992)

Crystals

Solubility · 2 Einträge

less than 1 mg/mL at 72 °F (NTP, 1992)

Partially soluble in ethanol and vegetable oils

DecompositionWhen heated to decomposition it emits toxic fumes of /nitrogen oxide/.
Melting Point · 2 Einträge

311 to 315 °F (NTP, 1992)

156 °C

Physikochemische Eigenschaften

Schmelzpunkt
155 · 155-157°
Siedepunkt
448.73 °C · 448.73°C (rough estimate)
Dichte
1.251 · 1.2510 (rough estimate)
Brechungsindex
1.57 · 1.5700 (estimate)
storage temp.
2 · 2-8°C
pka
13.61 · 13.61±0.50(Predicted)

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 6 Einträge

Warning

H351 (100%): Suspected of causing cancer [Warning Carcinogenicity]

P203, P280, P318, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 39 reports by companies from 2 notifications to the ECHA C&L Inventory.

Warning

H351: Suspected of causing cancer [Warning Carcinogenicity]

Gefahrenhinweise

Regulatory Information · 2 Einträge

Hazard Traits - Carcinogenicity

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

Fire HazardsFlash point data for this chemical are not available. It is probably combustible. (NTP, 1992)
Health HazardsACUTE/CHRONIC HAZARDS: When heated to decomposition it emits toxic fumes of NOx. (NTP, 1992)
Hazards SummaryIn chronic high-dose feeding studies of rats and mice: increased bladder stones and bladder carcinomas; [HSDB]
FDA RequirementsAll batches of this color additive when used as in food shall meet the specifications, uses and restrictions, and labeling regulations contained in 21 CFR Part 74 and be certified in accordance with regulations in 21 CFR Part 80.
Reactive GroupAzo, Diazo, Azido, Hydrazine, and Azide Compounds

Sicherheit und Schutzausrüstung

Fire FightingFires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
First Aid · 1 Eintrag

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

Storage Conditions · 1 Eintrag

PRECAUTIONS FOR "CARCINOGENS": Storage site should be as close as practical to lab in which carcinogens are to be used, so that only small quantities required for ... expt need to be carried. Carcinogens should be kept in only one section of cupboard, an explosion-proof refrigerator or freezer (depending on chemicophysical properties ...) that bears appropriate label. An inventory ... should be kept, showing quantity of carcinogen & date it was acquired ... Facilities for dispensing ... should be contiguous to storage area. /Chemical Carcinogens/

Cleanup Methods · 1 Eintrag

PRECAUTIONS FOR "CARCINOGENS": A high-efficiency particulate arrestor (HEPA) or charcoal filters can be used to minimize amt of carcinogen in exhausted air ventilated safety cabinets, lab hoods, glove boxes or animal rooms ... Filter housing that is designed so that used filters can be transferred into plastic bag without contaminating maintenance staff is avail commercially. Filters should be placed in plastic bags immediately after removal ... The plastic bag should be sealed immediately ... The sealed bag should be labelled properly ... Waste liquids ... should be placed or collected in proper containers for disposal. The lid should be secured & the bottles properly labelled. Once filled, bottles should be placed in plastic bag, so that outer surface ... is not contaminated ... The plastic bag should also be sealed & labelled. ... Broken glassware ... should be decontaminated by solvent extraction, by chemical destruction, or in specially designed incinerators. /Chemical Carcinogens/

Nonfire Spill Response · 1 Eintrag

SMALL SPILLS AND LEAKAGE: If you spill this chemical, you should dampen the solid spill material with water, then transfer the dampened material to a suitable container. Use absorbent paper dampened with water to pick up any remaining material. Seal your contaminated clothing and the absorbent paper in a vapor-tight plastic bag for eventual disposal. Wash all contaminated surfaces with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned.

Disposal Methods · 5 Einträge

SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in soil or water; effects on animal and plant life; and conformance with environmental and public health regulations.

PRECAUTIONS FOR "CARCINOGENS": There is no universal method of disposal that has been proved satisfactory for all carcinogenic compounds & specific methods of chem destruction ... published have not been tested on all kinds of carcinogen-containing waste. ... summary of avail methods & recommendations ... /given/ must be treated as guide only. /Chemical Carcinogens/

PRECAUTIONS FOR "CARCINOGENS": ... Incineration may be only feasible method for disposal of contaminated laboratory waste from biological expt. However, not all incinerators are suitable for this purpose. The most efficient type ... is probably the gas-fired type, in which a first-stage combustion with a less than stoichiometric air:fuel ratio is followed by a second stage with excess air. Some ... are designed to accept ... aqueous & organic-solvent solutions, otherwise it is necessary ... to absorb soln onto suitable combustible material, such as sawdust. Alternatively, chem destruction may be used, esp when small quantities ... are to be destroyed in laboratory. /Chemical Carcinogens/

PRECAUTIONS FOR "CARCINOGENS": HEPA (high-efficiency particulate arrestor) filters ... can be disposed of by incineration. For spent charcoal filters, the adsorbed material can be stripped off at high temp & carcinogenic wastes generated by this treatment conducted to & burned in an incinerator. ... LIQUID WASTE: ... Disposal should be carried out by incineration at temp that ... ensure complete combustion. SOLID WASTE: Carcasses of lab animals, cage litter & misc solid wastes ... should be disposed of by incineration at temp high enough to ensure destruction of chem carcinogens or their metabolites. /Chemical Carcinogens/

For more Disposal Methods (Complete) data for CITRUS RED 2 (6 total), please visit the HSDB record page.

Toxikologische Informationen

Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 2.3X10+4(SRC), determined from a structure estimation method(2), indicates that Citrus Red 2 is expected to be immobile in soil(SRC). Volatilization of Citrus Red 2 from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 5.2X10-13 atm-cu m/mole(SRC), using a fragment constant estimation method(3). Citrus Red 2 is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 3.0X10-9 mm Hg at 25 °C(SRC), determined from a fragment constant method(4). Biodegradation data in soil were not available(SRC, 2011).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 2.3X10+4(SRC), determined from a structure estimation method(2), indicates that Citrus Red 2 is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 5.2X10-13 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). According to a classification scheme(5), an estimated BCF of 10(SRC), from an estimated log Kow of 5.67(6) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Biodegradation data in water were not available(SRC,2011). However, Azo dyes, such as Citrus Red 2, are hydrophobic compounds, suggesting they will partition strongly to bottom sediments where reductive cleavage of the azo linkage may occur. This transformation process could result in the release of potentially hazardous aromatic amines to the water column(8), in this case 1-amino-2,5-dimethoxybenzene and 2-hydroxy-1-napthylamine(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), Citrus Red 2, which has an estimated vapor pressure of 3.0X10-9 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), is expected to exist solely in the particulate phase in the ambient atmosphere. Particulate-phase Citrus Red 2 may be removed from the air by wet or dry deposition(SRC). Citrus Red 2 contains chromophores that absorb at wavelengths >290 nm(3), and therefore may be susceptible to direct photolysis by sunlight(SRC).

Adverse EffectsIARC Carcinogen - Class 3: Chemicals are not classifiable by the International Agency for Research on Cancer.
Medical Surveillance · 1 Eintrag

PRECAUTIONS FOR "CARCINOGENS": Whenever medical surveillance is indicated, in particular when exposure to a carcinogen has occurred, ad hoc decisions should be taken concerning ... /cytogenetic and/or other/ tests that might become useful or mandatory. /Chemical Carcinogens/

Soil Adsorption/Mobility · 1 Eintrag

Using a structure estimation method based on molecular connectivity indices(1), the Koc of Citrus Red 2 can be estimated to be 2.3X10+4(SRC). According to a classification scheme(2), this estimated Koc value suggests that Citrus Red 2 is expected to be immobile in soil.

Artificial Pollution SourcesCitrus Red 2's production and use to color orange skins(1) may result in its release to the environment through various waste streams(SRC).
Environmental Biodegradation · 1 Eintrag

ANAEROBIC: Azo dyes are hydrophobic compounds, suggesting they will partition strongly to bottom sediments where reductive cleavage of the azo linkage may occur. This transformation process could result in the release of potentially hazardous aromatic amines to the water column(1), in this case 1-amino-2,5-dimethoxybenzene and 2-hydroxy-1-napthylamine(SRC).

Regulatorische Informationen

FDA RequirementsAll batches of this color additive when used as in food shall meet the specifications, uses and restrictions, and labeling regulations contained in 21 CFR Part 74 and be certified in accordance with regulations in 21 CFR Part 80.

Sicherheitsdaten

wgk
3
tsca
TSCA listed
RTECS-Nr.
QL3675000
risk_code
40
Toxizität
citrus red is a color used for coloring the skin of mature oranges. This compound has been described as being carcinogenic.
hazard_code
Xn

Chemie und Industrie

Pharmakologische Informationen

Metabolism/Metabolites · 5 Einträge

When citrus red number 2 was administered to rats with cannulated bile ducts, 6 red-colored, water-soluble metabolites were detected in bile, and traces of 1-amino-2-naphthol glucuronide and 1-amino-2-naphthol sulfate were present in urine.

1-Amino-2-naphthyl glucuronide is a metabolite of citrus red number 2 in humans.

The urine of normal rats dosed with the color contained 6 metabolites: 1 of the two red-colored metabolites was the O-glucuronide of citrus red number 2 (2,5-dimethoxyphenylazo-2-naphthyl glucuronide); two of the products were unidentified; two others were 1-amino-2-naphthol glucoronide and 1-amino-2-napthol sulfate. The urine of dogs given color contained 12 metabolites, one of which, 1-amino-2-naphthol sulfate, was present in high concentrations; however, 1-amino-2-napthyl glucoronide was not detected.

In vitro incubation of emulsions of the color with the intestinal contents of the rat, rabbit and dog resulted in destruction of the color by the bacterial flora.

Small amounts of 1-amino-2-naphthyl sulphate were identified in the urine of rats. This demonstrates that the color is reduced at the azo linkage in the animal body followed by conjugation to give the o-glucuronide and ethereal sulphate derivatives of 1-amino-2-naphthol.

Absorption, Distribution and Excretion · 2 Einträge

After single oral doses of 2-20 mg in corn oil solution to rats, five to seven percent of the administered color was recovered in the feces in 48 hr. When the dose was reduced to 0.5 mg no color was found. When administered as a 0.5 percent dry mixture, 26.3 percent was found in the feces. Rabbits and dogs showed similar results.

After a single dose small amounts of the color were found in the body fat. Repeated administration resulted in gradual reduction of the concentration of the color in the fat and finally it disappeared altogether after seven to 10 days.

Verwendung und Herstellung

Uses · 4 Einträge

Used formerly as dye for orange skins that are not processed; [HSDB]

Considered unsafe for food use by FAO/WHO committee in 1973; [HSDB]

To color orange skins

Citrus Red No. 2 shall be used only for coloring the skins of oranges that are not intended or used for processing (or if so used are designated in the trade as Packinghouse elimination) and that meet minimum maturity standards established by or under the laws of the States in which the oranges are grown.

Consumption Patterns100% AS DYE FOR COLORATION OF MATURE CITRUS FRUITS (E.G., ORANGES) (1974)
Methods of Manufacturing/Citrus Red No. 2/ is synthesized commercially by coupling diazotization of 2,5-dimethoxyaniline with 2-naphthol.
Formulations/PreparationsCitrus red number 2 used in food must contain minimum of 98% pure chemical (FAO/WHO, 1966; US Code of Federal Regulations, 1974).
Use ClassificationFood Additives -> COLOUR -> JECFA Functional Classes
General Manufacturing Information · 6 Einträge

2-Naphthalenol, 1-[2-(2,5-dimethoxyphenyl)diazenyl]-: ACTIVE

In USA, color is permitted only for coloring skins of oranges that are not intended or used for processing, at level not exceeding 2 ppm on basis of wt of the whole fruit. (US Code of Federal Regulations, 1974).

Color additives were initially regulated in the United States under the U.S. Department of Agriculture's (USDA) Bureau of Chemistry. In 1906, the Food and Drugs Act was passed by Congress, which prohibited the use of poisonous or deleterious colors in confectionery and the coloring or staining of food to conceal damage or inferiority. In 1927, responsibility of the Food and Drugs Act was transferred to FDA. Increasing government oversight, the Federal Food, Drug, and Cosmetic Act (FFDCA) was passed in 1938 and established the three following categories for colors: FD&C: colors used in foods, drugs and cosmetics; D&C: colors used in drugs and cosmetics when in contact with mucous membranes or ingested; and Ext. D&C: colors used in products applied externally.

The joint FAO/WHO expert committee on food additives ... considers citrus red number 2, on basis of toxicological evidence, to be unsafe for use in food (FAO/WHO, 1973).

This color should not be used as a food additive.

The US International Trade Commission last reported US production of Citrus Red 2 (Solvent Red 80) in 1970 by two US manufacturers (Allied Chemical Corp and American Cyanamid)

Anwendungen

VerwendenTo color orange skins.

Darstellung

synthetische2,5-Dimethoxyaniline diazotization, and Naphthalen-2-ol coupling.

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