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Home > Encyclopedia > Acid Red 114

Acid Red 114

Acid Red 114 structure

Acid Red 114 

structure
  • CAS No:

    6459-94-5

  • Formula:

    C37H30N4O10S3.2Na

  • Chemical Name:

    Acid Red 114

  • Synonyms:

    1,3-Naphthalenedisulfonic acid,8-[2-[3,3′-dimethyl-4′-[2-[4-[[(4-methylphenyl)sulfonyl]oxy]phenyl]diazenyl][1,1′-biphenyl]-4-yl]diazenyl]-7-hydroxy-,sodium salt (1:2);C.I. Acid Red 114,disodium salt;C.I. Acid Red 114;1,3-Naphthalenedisulfonic acid,8-[[3,3′-dimethyl-4′-[[4-[[(4-methylphenyl)sulfonyl]oxy]phenyl]azo][1,1′-biphenyl]-4-yl]azo]-7-hydroxy-,disodium salt;C.I. 23635;Acid Leather Red BG;Benzyl Fast Red BG;Benzyl Red BR;Erionyl Red RS;Fenafor Red PB;Folan Red B;Kayanol Milling Red RS;Leather Fast Red B;Midlon Red PRS;Milling Fast Red B;Milling Red B;Milling Red BB;Milling Red SWB;Polar Red RS;Sulphonol Red R;Suminol Milling Red RS;Supranol Fast Red GG;Supranol Red R;Supranol Red PBX-CF;Telon Fast Red GG;Tertracid Milling Red B;Vondamol Fast Red RS;Sella Fast Red RS;Levanol Red GG;Acid Red 114;Sandolan Red N-RS;Amacid Milling Red PRS;Supranol Fast Red 3G;Kayanol Milling Red RS 125;Everacid Milling Red RS;Sandolan Red N-RSI;Suminol Milling Red RS 125;Erionyl Red RS 125;Sandolan Red RSNI;Covanyl Scarlet RS;Pacid Red RS;Ratna Acid Red RS;Navimill Red RS;Monacid Red RS;Fabracid Red M-RS;Daedo Acid Red RS;Milling Fast Red R;Kenamide Red K 2R;Acid Milling Red BS;Simacid Red 24900;Acid Milling Red RS;Rifa Leather Red R;Multicuer Red R;Dinacid Milling Red RG;Covalene Red RS;Colomill Red RS;Acid Red RS;Everlan Red RS;Dycosweak Acid RS;Anadurm Red M-R;Concorde Leather Red RSN;471258-22-7

  • Categories:

    Dyes and Pigments  >  Dye

Description

solid


C.i. acid red 114 is a dark red powder. (NTP, 1992)


C.i. acid red 114 is a dark red powder. (NTP, 1992)|CI Acid red 114 is an organic molecular entity.

Acid Red 114 Basic Attributes

830.81

830.07600

229-272-0

P8TW4PSS87

DTXSID8021224

Red powder|Dark maroon powder /Dye content 45%/

3204120000

Characteristics

252.58000

11.78670

C.i. acid red 114 is a dark red powder. (NTP, 1992)

200-300 °C (decomposes)

less than 0.1 mg/mL at 72.5° F (NTP, 1992)

Keep container tightly closed in a dry and well-ventilated place. Avoid formation of dust and aerosols. Provide appropriate exhaust ventilation at places where dust is formed. Normal measures for preventive fire protection.|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/

Red to dark red solution in water|... bright red anionic bisazo dye

Azo dyes can be explosive when suspended in air at specific concentrations. This organic acid has a moderate soluble in water. The resulting solutions contain concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid.

Azo, Diazo, Azido, Hydrazine, and Azide Compounds

Explosive

C.I. ACID RED 114 is an azo compound. Toxic gases are formed by mixing compounds containing azo groups with acids, aldehydes, amides, carbamates, cyanides, inorganic fluorides, halogenated organics, isocyanates, ketones, metals, nitrides, peroxides, phenols, epoxides, acyl halides, and strong oxidizing or reducing agents. Flammable gases are formed by mixing materials in this group with alkali metals. Explosive combination can occur with strong oxidizing agents, metal salts, peroxides, and sulfides.

Safety Information

III

9

3077

40-45

22-36/37/39-45-53

QJ6475500

Xn,T

Stable. Incompatible with strong oxidizing agents.

P201-P308 + P313

H350

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.|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 C.I. Acid Red 114 (6 total), please visit the HSDB record page.

DHHS/NTP; Toxicology & Carcinogenesis Studies of C.I. Acid Red 114 in F344/N Rats (Drinking Water Studies) Technical Report Series No. 405 (1991) NIH Publication No. 92-3136|WHO/IARC Monograph on the Evaluation of the Carcinogenic Risks to Humans; Vol 57, Occupational Exposures of Hairdressers and Barbers and Personal Use of Hair Colourants; Some Hair Dyes, Cosmetic Colourants, Industrial Dyestuffs and Aromatic Amines, pp 247-257. IARC Monographs provide critical reviews of data on carcinogenicity for agents to which humans are known to be exposed and on specific exposure situations.[Available from, as of May 5, 2010: http://monographs.iarc.fr/index.php]

Flash point data for this chemical are not available; however, it is probably combustible. (NTP, 1992)

|Danger|H350 (88.37%): May cause cancer [Danger Carcinogenicity]|P201, P202, P281, P308+P313, P405, and P501|Aggregated GHS information provided by 53 companies from 5 notifications to the ECHA C&L Inventory.|H341: Suspected of causing genetic defects [Warning Germ cell mutagenicity]|Warning|H351: Suspected of causing cancer [Warning Carcinogenicity]|P201, P202, P260, P281, P308+P313, P314, P405, and P501

SMALL SPILLS AND LEAKAGE: If you spill this chemical, FIRST REMOVE ALL SOURCES OF IGNITION. You should then dampen the solid spill material with 60-70% methanol, then transfer the dampened material to a suitable container. Use absorbent paper dampened with methanol to pick up any remaining material. Your contaminated clothing and absorbent paper should be sealed in a vapor-tight plastic bag for eventual disposal. Solvent-wash contaminated surfaces with 60-70% methanol followed by washing 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. STORAGE PRECAUTIONS: You should store this material in a refrigerator. (NTP, 1992)

RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)|Handle with gloves. Safety glasses. Choose body protection according to the amount and concentration of the dangerous substance at the work place.|PRECAUTIONS FOR "CARCINOGENS": ... Dispensers of liq detergent /should be available./ ... Safety pipettes should be used for all pipetting. ... In animal laboratory, personnel should ... wear protective suits (preferably disposable, one-piece & close-fitting at ankles & wrists), gloves, hair covering & overshoes. ... In chemical laboratory, gloves & gowns should always be worn ... however, gloves should not be assumed to provide full protection. Carefully fitted masks or respirators may be necessary when working with particulates or gases, & disposable plastic aprons might provide addnl protection. ... Gowns ... /should be/ of distinctive color, this is a reminder that they are not to be worn outside the laboratory. /Chemical Carcinogens/

Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide. Wear self contained breathing apparatus for fire fighting if necessary.

Use personal protective equipment. Avoid dust formation. Avoid breathing dust. Ensure adequate ventilation. Do not let product enter drains. Pick up and arrange disposal without creating dust. Keep in suitable, closed containers for disposal.|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/

SRP: The scientific literature for the use of contact lenses by industrial workers is inconsistent. The benefits or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.|PRECAUTIONS FOR "CARCINOGENS": Smoking, drinking, eating, storage of food or of food & beverage containers or utensils, & the application of cosmetics should be prohibited in any laboratory. All personnel should remove gloves, if worn, after completion of procedures in which carcinogens have been used. They should ... wash ... hands, preferably using dispensers of liq detergent, & rinse ... thoroughly. Consideration should be given to appropriate methods for cleaning the skin, depending on nature of the contaminant. No standard procedure can be recommended, but the use of organic solvents should be avoided. Safety pipettes should be used for all pipetting. /Chemical Carcinogens/|PRECAUTIONS FOR "CARCINOGENS": In animal laboratory, personnel should remove their outdoor clothes & wear protective suits (preferably disposable, one-piece & close-fitting at ankles & wrists), gloves, hair covering & overshoes. ... Clothing should be changed daily but ... discarded immediately if obvious contamination occurs ... /also,/ workers should shower immediately. In chemical laboratory, gloves & gowns should always be worn ... however, gloves should not be assumed to provide full protection. Carefully fitted masks or respirators may be necessary when working with particulates or gases, & disposable plastic aprons might provide addnl protection. If gowns are of distinctive color, this is a reminder that they should not be worn outside of lab. /Chemical Carcinogens/|PRECAUTIONS FOR "CARCINOGENS": ... Operations connected with synth & purification ... should be carried out under well-ventilated hood. Analytical procedures ... should be carried out with care & vapors evolved during ... procedures should be removed. ... Expert advice should be obtained before existing fume cupboards are used ... & when new fume cupboards are installed. It is desirable that there be means for decreasing the rate of air extraction, so that carcinogenic powders can be handled without ... powder being blown around the hood. Glove boxes should be kept under negative air pressure. Air changes should be adequate, so that concn of vapors of volatile carcinogens will not occur. /Chemical Carcinogens/|For more Preventive Measures (Complete) data for C.I. Acid Red 114 (10 total), please visit the HSDB record page.

PRECAUTIONS FOR "CARCINOGENS": Procurement ... of unduly large amt ... should be avoided. To avoid spilling, carcinogens should be transported in securely sealed glass bottles or ampoules, which should themselves be placed inside strong screw-cap or snap-top container that will not open when dropped & will resist attack from the carcinogen. Both bottle & the outside container should be appropriately labelled. ... National post offices, railway companies, road haulage companies & airlines have regulations governing transport of hazardous materials. These authorities should be consulted before ... material is shipped. /Chemical Carcinogens/|PRECAUTIONS FOR "CARCINOGENS": When no regulations exist, the following procedure must be adopted. The carcinogen should be enclosed in a securely sealed, watertight container (primary container), which should be enclosed in a second, unbreakable, leakproof container that will withstand chem attack from the carcinogen (secondary container). The space between primary & secondary container should be filled with absorbent material, which would withstand chem attack from the carcinogen & is sufficient to absorb the entire contents of the primary container in the event of breakage or leakage. Each secondary container should then be enclosed in a strong outer box. The space between the secondary container & the outer box should be filled with an appropriate quantity of shock-absorbent material. Sender should use fastest & most secure form of transport & notify recipient of its departure. If parcel is not received when expected, carrier should be informed so that immediate effort can be made to find it. Traffic schedules should be consulted to avoid ... arrival on weekend or holiday ... /Chemical Carcinogens/

May cause eye irritation. May cause skin irritation. May cause respiratory tract irritation.

Toxicity

13 day studies: /F344/N/ rats were exposed to C.I. Acid Red 114 in drinking water at doses of 0, 10,000, 20,000, or 30,000 ppm. All control and dosed rats survived except one male rat in the 20,000 ppm dose group. Final mean body weights in the three dosed groups were 94%, 83%, or 77% of controls for males and 92%, 88%, or 80% of controls for females. Water consumption declined with increased dose. Clinical findings included red stained fur, ears, and tail in all test animals. On gross necropsy, organs and tissues were also stained red.|13 week studies: C.I. Acid Red 114 was administered /to F344N rats/ in drinking water at doses of 0, 600, 1,200, 2,500, 5,000, or 10,000 ppm. All control and dosed animals survived until the end of the study. Final mean body weights in the five dosed groups were 97%, 89%, 87%, 87%, or 85% of controls for males and 97%, 94%, 94%, 92%, or 89% of controls for females. Water consumption was decreased in dosed animals. As was seen in the 13 day studies, major organs and tissues from treated animals were stained red. Kidney toxicity characterized by regeneration and karyomegaly of tubule epithelial cells with chronic inflammation was observed in female rats at doses of 1,200 ppm or above. Treatment-related increases in relative liver weights and elevated liver enzyme levels were seen in males and females, centrilobular pallor in the liver was seen in all male dose groups. Because of these body weight differences, decreases in water consumption, and organ toxicity, the doses chosen for the 2 year studies were 70,150, and 300 ppm for males and 150, 300, and 600 for females.|Two year studies: Male /F344/N/ rats received doses of 0, 70, 150, or 300 ppm of C.I. Acid Red 114, and female /F344/N/ rats received 0, 150, 300, or 600 ppm. Seventy animals were in the control and high-dose groups, 45 in the low-dose groups, and 75 in the mid-dose groups. Ten animals were evaluated from the control and high-dose groups at 9 months, and ten animals from all dose groups were evaluated at 15 months. The average amount of compound consumed per day was 4, 8, or 20 mg/kg for males and 9, 20, or 70 mg/kg for females. Survival and Body Weights: Survival at 105 weeks for male rats receiving 0, 70, 150, or 300 ppm was 24/50, 15/35, 26/65, and 1/50; for females receiving 0, 150, or 300 ppm, survival was 36/50, 13/35, and 6/64. All female rats receiving 600 ppm died by week 89. The decreased survival in treated groups was due primarily to the development of chemical-related neoplasms. Of the surviving animals, the final mean body weights for males receiving 70 or 150 ppm were 94% and 90% of control and for females receiving 150 or 300 ppm, 99% and 84% of control. These weight differences began in the second year of the studies and were attributed in part to the development of neoplasms in the dosed groups. At 9 and 15 months, a few neoplasms were seen in the liver, lung, clitoral gland, skin, Zymbal's gland, oral cavity epithelium, and small and large intestine, and the number of neoplasms at these sites increased as the studies progressed. At 2 years, there was a clear carcinogenic response in the skin, Zymbal's gland, and liver of male and female rats, and in the clitoral gland, oral cavity epithelium, small and large intestine, and lung in female rats. Treatment-related increases were also seen in the incidence in neoplasms of the oral cavity epithelium, adrenal gland, and lung of male rats, and in mononuclear cell leukemia and in neoplasms of the mammary gland and adrenal gland in female rats. The incidence of these neoplasms was generally lower, but was significant and considered to be marginally related to chemical treatment. The same neoplastic effects have been previously observed in some or all of the NTP studies with dimethoxybenzidine, dimethylbenzidine, or C.I. Direct Blue 15.|In a standard preincubation protocol, C.I. Acid Red 114 was mutagenic in Salmonella typhimurium strain TA98 in the presence of induced hamster liver S9, and an equivocal response was noted in strain TA100 with hamster liver S9. However, no significant mutagenic activity was noted in strains TA1535 or TA1537 with or without S9 activation. In a modified S. typhimurium gene mutation test which employed reductive metabolism followed by oxidative metabolism with S9 liver enzymes, C.I. Acid Red 114 was strongly mutagenic in strain TA1538. C.I. Acid Red 114 did not induce sister chromatid exchanges or chromosomal aberrations in Chinese hamster ovary cells with or without S9 activation; reductive metabolism was not used in these cytogenetic tests. No increase in sex-linked recessive lethal mutations was observed in germ cells of male Drosophila melanogaster administered C.I. Acid Red 114 by feeding or injection.

C.I. Acid Red 114's production and use as a dye(1,2) may result in its release to the environment through various waste streams(SRC).

TERRESTRIAL FATE: Due to its ability to bind to surfaces, particularly to clay, by ion-exchange processes(1), and mineral surfaces such as goethite(2), C.I. Acid Red 114 is expected to absorb strongly to soils(SRC). Volatilization from moist soil is not expected because the acid exists as an ion and ions do not volatilize. Utilizing the Japanese MITI test, 1% of the Theoretical BOD was reached in 4 weeks(3) indicating that biodegradation is not an important environmental fate process under aerobic conditions. C.I. Acid Red 114 degraded 33-90% after 42 days in anaerobic sludge(4). These data indicate that anaerobic biodegradation may be an important fate process; however, the anaerobic reduction product, 3,3'-dimethylbenzidine, is classified as an A2 carcinogen(5).|AQUATIC FATE: Due to its ability to bind to surfaces, particularly to clay, by ion-exchange processes(1), and mineral surfaces such as goethite(2), C.I. Acid Red 114 is expected to absorb to aquatic soils and sediments(SRC). C.I. Acid Red 114 will exist almost entirely in ionic form at pH values of 5 to 9(3) and therefore volatilization from water surfaces is not expected to be an important fate process(SRC). According to a classification scheme(4), measured BCF ranges of 42-76 and 52-84(5) suggest that bioconcentration in aquatic organisms is moderate. Utilizing the Japanese MITI test, 1% of the Theoretical BOD was reached in 4 weeks(5) indicating that biodegradation is not an important environmental fate process under aerobic conditions. C.I. Acid Red 114 degraded 33-90% after 42 days in anaerobic sludge(6). These data indicate that anaerobic biodegradation may be an important fate process; however, the anaerobic reduction product, 3,3'-dimethylbenzidine, is classified as an A2 carcinogen(7).|ATMOSPHERIC FATE: C.I. Acid Red 114 is an ionic compound that will be essentially non-volatile in the environment(1,2). Therefore it is expected to exist solely in the particulate phase in the ambient atmosphere(SRC). Particulate-phase C.I. Acid Red 114 may be removed from the air by wet or dry deposition(SRC). C.I. Acid Red 114 absorbs light at 365 nm and 514 nm(3) and therefore may be susceptible to direct photolysis by sunlight(SRC).

C.I. Acid Red 114 contains a sulfonic acid ester functional group(SRC), which may be susceptible to hydrolysis under environmental conditions(1). C.I. Acid Red 114 showed a light precipitate in water with a calcium concentration of 10-3 M(2). C.I. Acid Red 114 absorbs light at 365 nm and 514 nm(3) and therefore may be susceptible to direct photolysis by sunlight(SRC).

Carp exposed to 0.2 mg/L and 0.02 mg/L of C.I. Acid Red 114 over an 8 week period had measured BCF values of 42-76 and 52-84, respectively(1). According to a classification scheme(2), this BCF suggests the potential for bioconcentration in aquatic organisms is moderate(SRC).

Due to its ionic nature, the retention of C.I. Acid Red 114 by ion-exchange processes(1), particularly on clay surfaces and adsorption at mineral surfaces such as geothite(2), indicates that it will be immobile in soil(SRC). It was noted during a biodegradation experiment that C.I. Acid Red 114 tended to adsorb onto sludge(3).

C.I. Acid Red 114 is an ionic compound(SRC). Therefore, it is not expected to undergo volatilization(1,2).

NIOSH (NOES Survey 1981-1983) has statistically estimated that 18,511 workers (352 of these were female) were potentially exposed to C.I. Acid Red 114 in the US(1). Occupational exposure to C.I. Acid Red 114 may occur through inhalation of dust and dermal contact with this compound at workplaces where C.I. Acid Red 114 is produced or used. Use data indicate that the general population may be exposed to C.I. Acid Red 114 via dermal contact by direct dyeing of wool and silk using consumer products containing C.I. Acid Red 114(SRC).

Drug Information

CI Acid Red 114 (100 mg/kg) containing less than 1% 3,3'-dimethylbenzidine as an impurity was administered once in the diet to two female mongrel dogs weighing 15 kg, and 48-hr urine was analyzed for 3,3' -dimethylbenzidine, the potential metabolic product. Excretion was found to be 0.04% of the dose of dye administered, which is in excess of what would be expected from the level of impurity; para-aminophenyl-paratoluenesulfonate was also identified as a urinary metabolite. The same dose of CI Acid Red 114 was also administered once to four male Sprague- Dawley rats by intragastric intubation; after 72 hr, only 0.01 % of the dose could be identified as 3,3'-dimethylbenzidine.

3,3'-Dimethoxybenzidine is structurally similar to benzidine, a known human carcinogen, and 3,3'- dimethylbenzidine, which is reasonably anticipated to be a human carcinogen. Like benzidine and 3,3'-dimethylbenzidine, 3,3'-dimethoxybenzidine is used to synthesize many dyes, by linking of various chromophores to the base chemical by azo linkages. The azo bonds of 3,3'-dimethoxybenzidine-based dyes are chemically similar regardless of the chromophore used, and they are easily broken by chemicals or enzymes via reduction to form free 3,3'- dimethoxybenzidine and free chromophore. A number of bacteria catalyze this process, including Escherichia coli, found in the human gastrointestinal tract. This reductive process also has been found in rats and dogs ... Quantitative evidence /showed/ that the two 3,3'-dimethoxybenzidine-based dyes studied both were nearly completely metabolized to free 3,3'-dimethoxybenzidine. Bacteria in the animals' gastrointestinal tract are thought to be the primary agents of this metabolism. 3,3'-Dimethoxybenzidine-based dyes are mutagenic in bacteria when tested with metabolic activation and an azo-reductive preincubation protocol. It is assumed that the reductive breakdown process forms 3,3'-dimethoxybenzidine, which is known to cause mutations in bacteria

Carcinogens

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. SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment. INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing. INGESTION: DO NOT INDUCE VOMITING. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. Be prepared to transport the victim to a hospital if advised by a physician. If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. IMMEDIATELY transport the victim to a hospital. (NTP, 1992)

/SRP:/ Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR if necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on the left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. /Poisons A and B/|/SRP:/ Basic treatment: Establish a patent airway (oropharyngeal or nasopharyngeal airway, if needed). Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if needed. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Monitor for shock and treat if necessary ... . Anticipate seizures and treat if necessary ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with 0.9% saline (NS) during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 mL/kg up to 200 mL of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool ... . Cover skin burns with dry sterile dressings after decontamination ... . /Poisons A and B/|/SRP:/ Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious, has severe pulmonary edema, or is in severe respiratory distress. Positive-pressure ventilation techniques with a bag valve mask device may be beneficial. Consider drug therapy for pulmonary edema ... . Consider administering a beta agonist such as albuterol for severe bronchospasm ... . Monitor cardiac rhythm and treat arrhythmias as necessary ... . Start IV administration of D5W /SRP: "To keep open", minimal flow rate/. Use 0.9% saline (NS) or lactated Ringer's if signs of hypovolemia are present. For hypotension with signs of hypovolemia, administer fluid cautiously. Watch for signs of fluid overload ... . Treat seizures with diazepam or lorazepam ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Poisons A and B/

8-((3,3'-dimethyl-4'-((4-(((4-methylphenyl)sulfonyl)oxy)phenyl)azo)(1,1'-biphenyl)-4-yl)azo)-7-hydroxy-1,3-naphthalenedisulfonic acid disodium salt

Acid Red 114 Use and Manufacturing

Methods of Manufacturing

Using 3, 3'-dimethylbenzidine, G salt, phenol and p-toluenesulfonyl chloride as raw materials, 3, 3'-dimethylbenzidine is firstly double-nitridated, and then coupled with G salt and phenol respectively, and finally Condensed with p-toluenesulfonyl chloride to obtain the product. After filtering, drying and crushing, the finished product is obtained.

Uses

Used for dyeing wool, silk and wool blends

Production

(1977) 1.09X10+8 GRAMS|(1979) 1.73X10+8 GRAMS|117 tons in 1975|Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#5251]

Technical grade CI Acid Red 114 is available in commercial mixtures containing 25-85% pure dye. Other typical ingredients include sodium chloride and mineraI oil.|Some trade names: Acid Leather Red BG; Amacid Miling Red PRS; Benzyl Fast Red BG; Benzyl Red BR; Elcacid Miling Fast Red RS; Erionyl Red RS; Fenafor Red PB; Folan Red B; Intrazone Red BR; Kayanol Miling Red RS; Leather Fast Red B; Levanol Red GG; Midlon Red PRS; Milling Fast Red B; Milling Red B; Miling Red BB; Milling Red SWB; Polar Red RS; Sandolan Red N-RS; Sella Fast Red RS; Sulphonol Red R; Suminol Miling Red RS; Supranol Fast Red 3G; Supranol Fast Red GG; Supranol Red PBX-CF; Supranol Red R; Telon Fast Red GG; Tertracid Milling Red B; Vondamol Fast Red RS.

1,3-Naphthalenedisulfonic acid, 8-[2-[3,3'-dimethyl-4'-[2-[4-[[(4-methylphenyl)sulfonyl]oxy]phenyl]diazenyl][1,1'-biphenyl]-4-yl]diazenyl]-7-hydroxy-, sodium salt (1:2): ACTIVE|... available in commercial mixtures containing 25-85% pure dye. Other typical ingredients include sodium chloride and mineral oil ... /Technical grade/

Health Hazards -> Carcinogens

Computed Properties

Molecular Weight:830.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:14
Rotatable Bond Count:8
Exact Mass:830.07629519
Monoisotopic Mass:830.07629519
Topological Polar Surface Area:253
Heavy Atom Count:56
Complexity:1620
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes

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