4680-78-8CCN(Cc1cccc(S(=O)(=O)[O-])c1)c1ccc(C(=C2C=CC(=[N+](CC)Cc3cccc(S(=O)(=O)[O-])c3)C=C2)c2ccccc2)cc1.[Na+]XKTMIJODWOEBKO-UHFFFAOYSA-MC.i. acid green 3 appears as a dull dark green powder. Used as a dye for silk or wool and biological stains.
A dull, dark green powder or bright crystalline solid
Maroon-purple powder
A dull, dark green powder or a bright, crystalline solid
In 2-methoxyethanol 20 mg/mL; in ethanol 9 mg/mL
In water, 30 mg/mL
C.i. acid green 3 appears as a dull dark green powder. Used as a dye for silk or wool and biological stains.
Wet Solid
Dark green solid; [Merck Index]
Soluble in water to a green solution which becomes brownish-yellow on addition of hydrochloric acid and blackish-green with sodium hydroxide. An excess of sodium hydroxide decolorizes the solution.
Sparingly soluble in alcohol; it dissolves in concentrated sulfuric acid to a yellow solution which, when diluted with water, turns first yellowish-red, then green.
安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
Chemical: Benzenemethanaminium, N-ethyl-N-[4-[[4-[ethyl[(3-sulfophenyl)methyl]amino]phenyl]phenylmethylene]-2,5-cyclohexadien-1-ylidene]-3-sulfo-, hydroxide, inner salt, sodium salt
Benzenemethanaminium, N-ethyl-N-[4-[[4-[ethyl[(3-sulfophenyl)methyl]amino]phenyl]phenylmethylene]-2,5-cyclohexadien-1-ylidene]-3-sulfo-, inner salt, sodium salt (1:1) is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Benzenemethanaminium, N-ethyl-N-[4-[[4-[ethyl[(3-sulfophenyl)methyl]amino]phenyl]phenylmethylene]-2,5-cyclohexadien-1-ylidene]-3-sulfo-, inner salt, sodium salt (1:1) are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
C.I. ACID GREEN 3 neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. May generate hydrogen, a flammable gas, in combination with strong reducing agents such as hydrides.
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.
Used to dye wool, silk, leather, and paper; Also used in wood stains, biological stains, and, indicators; Used as a cosmetic in Western Europe (no contact with mucous membranes) and in Japan (external use only); [HSDB]
Discontinued use as a color additive for foods, drugs and cosmetics in the US in 1966; [HSDB]
Pulp and Paper Processing [Category: Industry]
Limited use as a dye for silk and wool fabrics; as biological stain
Use in barium and aluminum lakes that are used as pigments, in wood stain and in paper dyes.
Because of its low lightfastness ... has limited application in both dyeing and printing wool and silk (from an acid bath). Although it dyes fully chromed leather a brilliant green, this application ... is flawed by a low lightfastness.
2023: 141,000 lb
(1973) approx 93,500 kg
Food Additives -> COLOUR -> JECFA Functional Classes
Food Additives -> COLOUR -> JECFA Functional Classes
Food Additives -> COLOUR -> JECFA Functional Classes
読み込み中…
4680-78-8DTXSID3020671CHEMBL1333604CHEBI:90112化学的特性Green powder
LC50; Species: Oryzias latipes (Medaka) length 2 cm, weight 0.2 g; Conditions: freshwater, static, 25 °C; Concentration: 1000000 ug/L for 24 hr /formulation/
LC50; Species: Oryzias latipes (Medaka) length 2 cm, weight 0.2 g; Conditions: freshwater, static, 25 °C; Concentration: 990000 ug/L for 48 hr /formulation/
TERRESTRIAL FATE: Acid dyes, such as C.I. Acid Green 3, typically exhibit very low solubilities in octanol and have water solubilities that exceed 100 g/L. Therefore, these compounds would be expected to remain in the water column in the aquatic environment and show little affinity for organic matter(1) which suggests a potential to leach in soil(SRC). Volatilization of C.I. Acid Green 3 from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 4.9X10-29 atm-cu m/mole(SRC), using a fragment constant estimation method(2). C.I. Acid Green 3 not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 7.2X10-39 mm Hg at 25 °C(SRC), determined from a fragment constant method(2). Biodegradation data in soil were not available(SRC, 2011).
AQUATIC FATE: Acid dyes, such as C.I. Acid Green 3, typically exhibit very low solubilities in octanol and have water solubilities that exceed 100 g/L. Therefore, these compounds would be expected to remain in the water column in the aquatic environment and show little affinity for organic matter(1). Volatilization from water surfaces is not expected(2) based upon an estimated Henry's Law constant of 4.9X10-29 atm-cu m/mole(SRC), developed using a fragment constant estimation method(3). According to a classification scheme(4), an estimated BCF of 3(SRC), from an estimated log Kow of -3.20(3) and a regression-derived equation(3), suggests the potential for bioconcentration in aquatic organisms is low(SRC). Biodegradation data in water were not available(SRC, 2011).
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), C.I. Acid Green 3, which has an estimated vapor pressure of 7.2X10-39 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 C.I. Acid Green 3 may be removed from the air by wet or dry deposition(SRC). C.I. Acid Green 3 absorbs light at wavelengths of 618 nm(4), and therefore may be susceptible to direct photolysis by sunlight(SRC).
Acid dyes, such as C.I. Acid Green 3, typically exhibit very low solubilities in octanol and have water solubilities that exceed 100 g/L. Therefore, these compounds would be expected to remain in the water column in the aquatic environment and show little affinity for organic matter(1).
/OTHER TOXICITY INFORMATION/ Most organic azo dyes are potential skin sensitizers, the most important of which are paraphenylenediamine and its analogs. Water soluble azo dyes are more likely to cause clinical sensitization than insoluble dyes. ... In addition to allergic eczematous contact dermatitis, color developing solutions have caused lichen planus like eruptions. /Organic dyes/
Guinea Green B
Group 3: Not classifiable as to its carcinogenicity to humans
Volume 16: (1978) Some Aromatic Amines and Related Nitro Compounds – Hair Dyes, Colouring Agents and Miscellaneous Industrial Chemicals
1987
1987
An estimated BCF of 3 was calculated in fish for C.I. Acid Green 3(SRC), using an estimated log Kow of -3.20(1) and a regression-derived equation(1). According to a classification scheme(2), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).
The Henry's Law constant for C.I. Acid Green 3 is estimated as 4.9X10-29 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that C.I. Acid Green 3 is expected to be essentially nonvolatile from water surfaces(2). C.I. Acid Green 3's Henry's Law constant indicates that volatilization from moist soil surfaces is not expected occur(SRC). C.I. Acid Green 3 is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 7.2X10-39 mm Hg(SRC), determined from a fragment constant method(1).
/LABORATORY ANIMALS: Acute Exposure/ Acid green was not damaging in rabbit eye test. It caused no more than slight transient irritation when tested on the eyes of rabbits, either by application of 4-8 mg of powdered dye to the conjunctival sac or by irrigating the surface of the eye for ten minutes with 0.02 M solution near neutrality after the epithelium has been removed to facilitate penetration. ...
/LABORATORY ANIMALS: Acute Exposure/ Arylmethane dyes which have been utilized as food colors, commercial dyes, laboratory stains and pH indicators were tested in the Salmonella/mammalian microsome mutagenicity assay. Eight mutagenic dyes were identified, including 5 food colors and 3 common laboratory stains; none of the 11 indicator dyes tested were mutagenic. The food color ... guinea green C.I. 42085 ... /was/ mutagenic in frameshift mutation detector strains TA98 and/or TA1538 and required metabolic activation. Most of the compounds gave weak mutagenic responses with Salmonella and were positive only within narrow dose ranges. Since conflicting results were obtained using dyes from different sources, minor dye components may have been responsible for their mutagenicity. Impurities in arylmethane colors still used in food and the toxicological role of such impurities merits further study.
/LABORATORY ANIMALS: Chronic Exposure or Carcinogenicity/ Toxicological testing of food dyes was conducted with experimental rats. ... Green-No-2 fed to rats at 2 percent of the diet for two years caused no tumors. With the remaining four dyes, Green-No-1 (Guinea-Green-B), Red-No-2 (amaranth), Red-No-3 (erythrosine), and Yellow-No-5 (tartrazine), no distant tumors were caused by the injections; except for one with Green-No-1, none appeared at the point of injection. Some of the animals survived, and feeding studies on some of the dyes were continued.
/LABORATORY ANIMALS: Chronic Exposure or Carcinogenicity/ The results of feeding rats, dogs and mice diets containing Guinea Green B, Light Green SF Yellowish or Fast Green FCF for 2 yr are reported. ... The three green colorings, Guinea Green B, Light Green SF Yellowish and Fast Green FCF, were each fed at dietary levels of 0.0, 1.0 and 2.0 % to groups of two male and two female beagle dogs for 2 yr. Ten of the 12 dogs fed Guinea Green B survived in good clinical condition. A male at 2 % was killed after 1 yr when he became moribund and a female at 1% died after 5 months. Both non-survivors showed generalized inanition-type atrophy of the bone marrow, fat, skeletal muscle, adrenal cortex, lymphatic tissue and the gastric mucosa. Moderate periportal fatty metamorphosis of the liver was observed in a male survivor on 2 %. ...
For more Non-Human Toxicity Excerpts (Complete) data for C.I. ACID GREEN 3 (11 total), please visit the HSDB record page.
Benzenemethanaminium, N-ethyl-N-[4-[[4-[ethyl[(3-sulfophenyl)methyl]amino]phenyl]phenylmethylene]-2,5-cyclohexadien-1-ylidene]-3-sulfo-, inner salt, sodium salt (1:1): ACTIVE
Guinea Green B has been produced commercially in the USA for over fifty years. Guinea green B was first produced commercially in Japan in 1940. It is believed that there is one producer currently; however, no production has been reported since 1973, when 200 kg were manufactured. There are no Japanese exports or imports of this chemical.
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.
使用Limited use as a dye for silk and wool fabrics; as biological stain.
一般的な説明A dull dark green powder. Used as a dye for silk or wool and biological stains.
製造方法Benzaldehyde (1 Moore) and 3-(Ethyl(phenyl)amino)methyl)benzenesulfonic acid (2 Moore) condensation, will product oxidation, and then translate into sodium salt.
定義ChEBI: An organic sodium salt having 3-[(ethyl{4-[(4-{ethyl[(3-sulfonatophenyl)methyl]amino}phenyl)(phenyl)methylidene]cyclohexa-2,5-dien-1-ylidene}azaniumyl)methyl]benzene-1-sulfonate. Used as a substitute for Light green SF yellowish in Masson's trichrome, alth ugh it is prone to fade. Previously used as a food dye but is now no longer approved.