2-Aminophenol
-
2-Aminophenol
structure -
-
CAS No:
95-55-6
-
Formula:
C6H7NO
-
Chemical Name:
2-Aminophenol
-
Synonyms:
Phenol,2-amino-;Phenol,o-amino-;2-Aminophenol;C.I. 76520;o-Aminophenol;BASF Ursol 3GA;Benzofur GG;C.I. Oxidation Base 17;Fouramine OP;Nako Yellow 3GA;Paradone Olive Green B;Pelagol 3GA;Pelagol Grey GG;Zoba 3GA;o-Hydroxyaniline;o-Hydroxyphenylamine;1-Amino-2-hydroxybenzene;1-Hydroxy-2-aminobenzene;2-Hydroxyaniline;2-Hydroxybenzenamine;o-Aminohydroxybenzene;Rodol 2G;NSC 1534;NSC 226261;(2-Hydroxyphenyl)amine;2-Amino-1-hydroxybenzene;2-Aminophenyl alcohol
- Categories:
-
CAS No:
Description
o-Aminophenol appears as colorless needles or as white crystalline substance turning tan to brown on exposure to air. Colorless to light yellow liqui
O-aminophenol appears as off-white crystals or beige powder. (NTP, 1992)|COLOURLESS-TO-WHITE CRYSTALS. TURNS DARK ON EXPOSURE TO AIR OR LIGHT.
O-aminophenol appears as off-white crystals or beige powder. (NTP, 1992)|2-aminophenol is the aminophenol which has the single amino substituent located ortho to the phenolic -OH group. It has a role as a bacterial metabolite.
2-Aminophenol Basic Attributes
109.13
109.13
606075
202-431-1
23RH73DZ65
0824
1534
2512
DTXSID8024498
Crystals, rapidly becoming brown|White orthorhombic bipyramidal needles from benzene or water|White crystals; turn brown with age|COLORLESS RHOMBIC NEEDLES OR PLATES
29222900
Characteristics
46.2
0.62
White to brown Powder
1.328 g/cm3 @ Temp: 25 °C
170-174 °C
100 °C @ Press: 1 x 10-3-3 x 10-3 Torr
168 °C
1.637
H2O: 17 g/L (20 ºC)
Store below +30°C.
negligible
Relative vapour density (air = 1): 3.77
Oral-rat LD50: 1300 mg/kg; Oral-Mouse LD50: 1250 mg/kg
Flammable; burning produces toxic nitrogen oxide fumes
4.84(at 20 °C)
Henry's Law constant = 2X10-10 atm-cu m/mole at 25 °C (est)
4.84 (at 20 °C)|pKa = 4.84 (conjugate acid)|pK1 = 4.72 at 21 °C; pK2 = 9.71 at 22 °C|pKa1 = 5.22 (amine); pKa2 = 9.87 (phenol) (est)
118.3 Ų [M+H]+ [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|124.8 Ų [M+H]+ [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|118 Ų [M-H]- [CCS Type: DT, Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]|118.3 Ų [M-H]-
At reduced pressure (1.47 kPa), 2-aminophenol sublimes rapidly at 153 °C without decomposition|Heat of formation = -191 kJ/mol|LOW VOLATILITY|Crystals readily becoming gray on exposure to light. Freely soluble in water or alcohol /o-Aminophenol hydrochloride/|Hydroxyl radical reaction rate constant = 7.4X10-11 cu cm/molecule-sec at 25 °C (est)
Protect from air and light. Insoluble in water.
Phenols and Cresols
O-AMINOPHENOL can react with oxidizing agents. (NTP, 1992) THF forms explosive products with 2-aminophenol [Lewis 3227].
190 °C
Safety Information
III
6.1
UN 2512 6.1/PG 3
2
20/22-68-34-20/21/22
28-36/37-28A-45-36/37/39-26-68-20/22
SJ4950000
Xn,C
Warehouse ventilated, low temperature and dry
Stable, but may be air or light sensitive. Incompatible with strong oxidizing agents.
P261-P280-P301 + P312 + P330
H302 + H332-H341
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.|Incineration. /Aminophenols/
Incompatible with acids, acid chlorides, and anhydrides, chloroformates, strong oxidizing agents.|Strong oxidants. /Aminophenols/
European Commission, ESIS; IUCLID Dataset, 2-Aminophenol (95-55-6) (2000 CD-ROM edition).[Available from, as of June 7, 2010: http://esis.jrc.ec.europa.eu/]|Elder RL; J Am Coll Toxicol 7 (3): 279-334 (1988). Final report on the safety assessment of p-aminophenol, m-aminophenol & o-aminophenol. Review liver, immune system, reproduction, mutagenicity, embryotoxicity, kinetics, methemoglobinemia, renal tubular necrosis, photosensitization, skin irritation, eye irritation, & carcinogenicity of hair dye.
Excerpt from ERG Guide 152 [Substances - Toxic (Combustible)]: Combustible material: may burn but does not ignite readily. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form. (ERG, 2016)|Combustible. Gives off irritating or toxic fumes (or gases) in a fire.
|Warning|H302: Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P261, P264, P270, P271, P281, P301+P312, P304+P312, P304+P340, P308+P313, P312, P330, P405, and P501|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|Aggregated GHS information provided by 2338 companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|Danger|P260, P261, P264, P270, P272, P273, P280, P301+P312, P302+P352, P314, P321, P330, P333+P313, P363, P391, and P501|P201, P202, P260, P261, P264, P270, P272, P280, P281, P301+P312, P302+P352, P308+P313, P309+P311, P314, P321, P330, P333+P313, P363, P405, and P501
Excerpt from ERG Guide 152 [Substances - Toxic (Combustible)]: As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. SPILL: Increase, in the downwind direction, as necessary, the isolation distance shown above. FIRE: If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. (ERG, 2016)
SMALL SPILLS AND LEAKAGE: Should a spill occur while you are handling this chemical, you should dampen the solid spill material with alcohol, then transfer the dampened material to a suitable container. Use absorbent paper dampened with alcohol to pick up any remaining material. Seal the absorbent paper, and any of your clothes, which may be contaminated, in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with alcohol followed by washing with a strong soap and water solution. Do not reenter the contaminate 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)
MINIMUM PROTECTIVE CLOTHING: When working with this chemical, you should wear impervious coveralls, shoe covers and gloves. 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. RECOMMENDED GLOVE MATERIALS: Permeation data indicate that polyvinyl chloride gloves may provide protection to contact with this compound. Polyvinyl chloride over latex gloves is recommended. However, if this chemical makes direct contact with your gloves remove them at once. (NTP, 1992)|Wear protective gloves and clothing to prevent any reasonable probability of skin contact ... Wear dust-proof chemical goggles and face shield unless full facepiece respiratory protection is worn. /Aminophenols/|P3 filter respirator for toxic particles.
Combustible
Use dry chemical, carbon dioxide, or alcohol foam extinguishers. Vapors are heavier than air and will collect in low areas. Vapors may travel long distances to ignition sources and flashback. Vapors in confined areas may explode when exposed to fire. Storage containers and parts of containers may rocket great distances, in many directions. If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters. Notify local health and fire officials and pollution control agencies. From a secure, explosion-proof location, use water spray to cool exposed containers. If cooling streams are ineffective (venting sound increases in volume and pitch, tank discolors or shows any signs of deforming), withdraw immediately to a secure position ... The only respirators recommended for fire fighting are self-contained breathing apparatuses that have full facepieces and are operated in a pressure-demand or other positive-pressure mode. /Anisidines/|If material on fire or involved in fire: Extinguish fire using agent suitable for type of surrounding fire. (Material itself does not burn or burns with difficulty.) Use water in flooding quantities as fog. Use foam, dry chemical, or carbon dioxide. Keep run-off water out of sewers and water sources. /Aminophenols/
Spill handling: keep dust under control. Use a vacuum or wet method to reduce dust during clean-up. Do not sweep. Evacuate persons not wearing protective equipment from area of spill or leak until clean-up is complete. Remove all ignition sources. Collect powdered material in the most convenient and safe manner and deposit in sealed containers. Ventilate area after clean-up is complete. It may be necessary to contain and dispose of this chemical as a hazardous waste. If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters. Contact your Department of Environmental Protection of your regional office of the federal EPA for specific recommendations. /Aminophenols/
... Disposable natural rubber latex gloves and disposable PVC gloves should not be used repeatedly for handling the hair dye products /p-aminophenol, m-aminophenol, o-aminophenol, and p-phenylenediamine/.|If material not on fire and not involved in fire: Keep sparks, flames, and other sources of ignition away. Keep material out of water sources and sewers. /Aminophenols/|Personnel protection: Avoid breathing dusts, and fumes from burning material. Keep upwind ... Avoid bodily contact with the material ... Do not handle broken packages unless wearing appropriate personal protective equipment. /Aminophenols/|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.
/GUIDE 152: SUBSTANCES - TOXIC (COMBUSTIBLE)/ Health: Highly toxic, may be fatal if inhaled, swallowed or absorbed through skin. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution. /Aminophenols/|/GUIDE 152: SUBSTANCES - TOXIC (COMBUSTIBLE)/ Fire or Explosion: Combustible material: may burn but does not ignite readily. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form. /Aminophenols/|/GUIDE 152: SUBSTANCES - TOXIC (COMBUSTIBLE)/ Public Safety: CALL Emergency Response Telephone Number ... . As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. Keep unauthorized personnel away. Stay upwind. Keep out of low areas. /Aminophenols/|/GUIDE 152: SUBSTANCES - TOXIC (COMBUSTIBLE)/ Protective Clothing: Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible. /Aminophenols/|For more DOT Emergency Guidelines (Complete) data for 2-Aminophenol (8 total), please visit the HSDB record page.
No person may /transport,/ offer or accept a hazardous material for transportation in commerce unless that person is registered in conformance ... and the hazardous material is properly classed, described, packaged, marked, labeled, and in condition for shipment as required or authorized by ... /the hazardous materials regulations (49 CFR 171-177)./|The International Air Transport Association (IATA) Dangerous Goods Regulations are published by the IATA Dangerous Goods Board pursuant to IATA Resolutions 618 and 619 and constitute a manual of industry carrier regulations to be followed by all IATA Member airlines when transporting hazardous materials.|The International Maritime Dangerous Goods Code lays down basic principles for transporting hazardous chemicals. Detailed recommendations for individual substances and a number of recommendations for good practice are included in the classes dealing with such substances. A general index of technical names has also been compiled. This index should always be consulted when attempting to locate the appropriate procedures to be used when shipping any substance or article.
May cause eye irritation. May cause skin irritation. May cause respiratory tract irritation.
Personal protection: chemical protection suit and particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Sweep spilled substance into covered sealable containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations.
Store in an area without drain or sewer access. Well closed. Separated from oxidants and food and feedstuffs.
A harmful concentration of airborne particles can be reached quickly when dispersed, especially if powdered.
The substance may cause effects on the blood. This may result in the formation of methaemoglobin. The effects may be delayed. Medical observation is indicated.
Repeated or prolonged contact may cause skin sensitization.
NO open flames.
STRICT HYGIENE!
Use local exhaust or breathing protection.
Protective gloves. Protective clothing.
Wear safety goggles.
| 1 - Materials that, under emergency conditions, can cause significant irritation.| 1 - Materials that must be preheated before ignition can occur. Materials require considerable preheating, under all ambient temperature conditions, before ignition and combustion can occur.| 0 - Materials that in themselves are normally stable, even under fire conditions.
Toxicity
moderately toxic
An investigation was carried out of the effects of ortho-aminophenol (95556) (o-AP), meta-aminophenol (591275) (m-AP), para-aminophenol (123308) (p-AP) & acetaminophen (103902) (AAP) on the induction of preneoplastic lesions in the liver & kidney of male Fischer-344-rats by N-ethyl-N-hydroxyethylnitrosamine (13147256) (EHEN). The rats in this 52 wk investigation included those give 0.1% EHEN in their drinking water for 2 wk & then, beginning 1 wk later, given 0.8% of either o-AP, m-AP, p-AP or AAP in the basal diet for 49 wk; those given EHEN & thereafter only the basal diet; & those given one of the test cmpds without prior EHEN admin. Body, liver & kidney weights were determined for sacrificed rats, & liver sections were subjected to immunohistochemical exam of glutathione-S-transferase placental type (GSTP) positive foci. The numbers of GSTP positive foci in the liver were significantly decreased in rats given o-AP, m-AP, p-AP or AAP after EHEN as compared to values for rats given EHEN alone. However, lowered incidences of GSTP positive foci were observed only in rats given o-AP or AAP after EHEN. Only p-AP & AAP gave significantly higher incidences of microadenoma & adenoma in the kidney.
LD50 Rat oral 1300 mg/kg|LD50 Rat sc 37 mg/kg|LD50 Mouse oral 1250 mg/kg|LD50 Mouse ip 200 mg/kg
/BIRDS and MAMMALS/ Ip injection of 50 mg/kg /of 2-Aminophenol/ in Japanese quail produced a peak of 25% methemoglobin in the blood after 10 min.
2-Aminophenol's production and use as a dyeing agent for furs, hair(1,2) and leather(2) and in the manufacturing of pharmaceuticals(1) may result in its release to the environment through various waste streams(SRC).
TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 90(SRC), determined from a structure estimation method(2), indicates that 2-aminophenol is expected to have high mobility in soil(SRC). However, anilines are expected to bind strongly to humus or organic matter in soils due to the high reactivity of the aromatic amino group(3,4), suggesting that mobility may be much lower in some soils(SRC). Measured pKa values are 4.72 and 9.71(5), for the amine and hydroxy functional groups, respectively(6); 2-aminophenol is amphoteric and behaves either as a weak acid or weak base; the basic character usually predominates(5). Volatilization of 2-aminophenol from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 2X10-10 atm-cu m/mole(SRC), using a fragment constant estimation method(7). 2-Aminophenol is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 5X10-4 Hg at 25 °C(SRC), determined from a fragment constant method(8). Based on screening tests, 2-aminophenol is expected to biodegrade; when present at 100 mg/L, in a respirometry screening test using an activated sludge inoculum, 45% of the theoretical BOD was reached in 10 days(9). A rate constant of 0.279X10-2 per hour was measured for 2-aminophenol in a screening test using a non-adapted activated sludge inoculum(10). Under denitrifying conditions in sediment, 2-aminophenol was mineralized following a long lag phase at a rate of 12.9 umol/L/day(11). It was not mineralized under methanogenic conditions in a 26-week sediment grab sample study(11).|AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 90(SRC), determined from a structure estimation method(2), indicates that 2-aminophenol 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 2X10-10 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). According to a classification scheme(5), an estimated BCF of 3(SRC), from its log Kow of 0.62(6) and a regression-derived equation(2), suggests the potential for bioconcentration in aquatic organisms is low(SRC). 2-Aminophenol is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(3). Based on screening tests, 2-aminophenol is expected to biodegrade when present at 100 mg/L, in a respirometry screening test using an activated sludge inoculum, 45% of the theoretical BOD was reached in 10 days(7). A rate constant of 0.279X10-2 per hour was measured for 2-aminophenol in a screening test using a non-adapted activated sludge inoculum(8). Under denitrifying conditions in sediment, 2-aminophenol was mineralized following a long lag phase at a rate of 12.9 umol/L/day(9). It was not mineralized under methanogenic conditions in a 26-week sediment grab sample study(9).|ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), 2-aminophenol, which has an estimated vapor pressure of 5.0X10-4 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase 2-aminophenol is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 5 hours(SRC), calculated from its rate constant of 7.4X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Particulate-phase 2-aminophenol may be removed from the air by wet or dry deposition(SRC). 2-Aminophenol absorbs light at wavelengths 281 nm(4) and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC).
The rate constant for the vapor-phase reaction of 2-aminophenol with photochemically-produced hydroxyl radicals has been estimated as 7.4X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1). This corresponds to an atmospheric half-life of about 5 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1). 2-Aminophenol is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(2). The reaction of hydroxyl radicals with neutral solutions of 2-aminophenol results in the formation of the 2-aminophenoxyl radical(3). 2-Aminophenol absorbs light at wavelengths of 281 nm(4) and therefore is not expected to be susceptible to direct photolysis by sunlight(SRC). 2-Aminophenol is expected to undergo fairly rapid oxidation in the presence of air(4). Measured pKa values are 4.72 and 9.71(4), for the amine and hydroxy functional groups, respectively(5); 2-aminophenol is amphoteric and behaves either as a weak acid or weak base; the basic character usually predominates(4).
An estimated BCF of 3 was calculated in fish for 2-aminophenol(SRC), using a log Kow of 0.62(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).
Using a structure estimation method based on molecular connectivity indices(1), the Koc of 2-aminophenol can be estimated to be 90(SRC). According to a classification scheme(2), this estimated Koc value suggests that 2-aminophenol is expected to have high mobility in soil. However, anilines are expected to bind strongly to humus or organic matter in soils due to the high reactivity of the aromatic amino group(3-4), suggesting that mobility may be much lower in some soils(SRC). Measured pKa values are 4.72 and 9.71(5), for the amine and hydroxy functional groups, respectively(6); 2-aminophenol is amphoteric and behaves either as a weak acid or weak base; the basic character usually predominates(5). At pH 8.4, 25.5% of added 2-aminophenol is sorbed by an organoclay(7). The sorptive capacity of clays for amine-substituted phenolic sorbate decreased with increasing pH above the corresponding pKa(8).
The Henry's Law constant for 2-aminophenol is estimated as 2X10-10 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that 2-aminophenol is expected to be essentially nonvolatile from water surfaces(2). 2-Aminophenol is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 5.0X10-4 mm Hg(SRC), determined from a fragment constant method(3).
According to the 2006 TSCA Inventory Update Report, the number of workers reasonably likely to be exposed in the industrial manufacturing, processing, and use of 2-aminophenol is 1 to 99 persons; the data may be greatly underestimated(1).|NIOSH (NOES Survey 1981-1983) has statistically estimated that 19,664 workers (14,753 of these were female) were potentially exposed to 2-aminophenol in the US(1). Occupational exposure to 2-aminophenol may occur through dermal contact with this compound at workplaces where 2-aminophenol is produced or used(SRC). Use data indicate that the general population may be exposed to 2-aminophenol via dermal contact with consumer products, particularly hair dye products, containing 2-aminophenol(SRC).
Drug Information
Recovery in urine for 24 hr of a single oral dose of 1 g in rabbits (strain and sex not given) was 95% of the administered dose ...|The substance can be absorbed into the body by ingestion, through the skin and by inhalation of its aerosol.
Recovery in urine for 24 hr of a single oral dose of 1 g in rabbits (strain and sex not given) was 95% of the administered dose: 11% unchanged o-aminophenol, 2-4% acetamidophenol, 15% aminophenolsulfate, 52% aminophenylglucuronide, 13% acetamidophenylglucuronide.|Yields 3-aminoacetechol in rabbit; yields o-aminophenyl-beta-glucuronide in guinea pig, mouse, rabbit; yields o-aminophenylsulfate in rabbit, mouse; yields 4-aminoresorcinol probably in rabbit.|Yields 3-aminoacetechol in rabbit. Yields o-aminophenyl-beta-d-glucuronide in guinea pig, mouse, rabbit. /From table/|Yields o-aminophenyl sulfate in rabbit, mouse. Yields 4-aminoresorcinol probably in rabbit. /From table/|For more Metabolism/Metabolites (Complete) data for 2-Aminophenol (8 total), please visit the HSDB record page.
SYMPTOMS: Symptoms of exposure to this compound include redness of the skin, coughing, and nausea. ACUTE/CHRONIC HAZARDS: Very toxic. May cause irritation on contact. Hazardous decomposition. (NTP, 1992)
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. Phenols are very toxic poisons AND corrosive and irritating, so that inducing vomiting may make medical problems worse. IMMEDIATELY call a hospital or poison control center and locate activated charcoal, egg whites, or milk in case the medical advisor recommends administering one of them. If advice from a physician is not readily available and the victim is conscious and not convulsing, give the victim a glass of activated charcoal slurry in water or, if this is not available, a glass of milk, or beaten egg whites and IMMEDIATELY transport victim to a hospital. If the victim is convulsing or unconscious, do not give anything by mouth, assure 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)
Fresh air, rest. Refer for medical attention.
Rinse and then wash skin with water and soap.
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
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 as necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on 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. /Aniline and related compounds/|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 necessary. Administer oxygen by nonrebreather mask at 10 to 15 L/min. 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 patent can swallow, has a strong gag reflex, and does not drool. Administer activated charcoal ... . /Aniline and related compounds/|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. 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 (LR) if signs of hypovolemia are present. For hypotension with signs of hypovolemia, administer fluid cautiously. Consider vasopressors if hypotensive with a normal fluid volume. Watch for signs of fluid overload ... . Administer 1% solution methylene blue if patient is symptomatic with severe hypoxia, cyanosis, and cardiac compromise not responding to oxygen. ... . Treat seizures with diazepam or lorazepam ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Aniline and related compounds/
/SIGNS AND SYMPTOMS/ Short term exposure: Aminophenols can be absorbed through the skin, thereby increasing exposure. Can cause lung irritation. Poisonous if swallowed. These chemicals lower the blood's ability to carry oxygen (methemoglobinemia). This condition causes a bluish color to the skin and lips, headaches, dizziness; higher exposures can result in unconsciousness and death. Irritates eyes, skin, and respiratory tract. Skin contact can cause burning sensation and rash ... May produce dermatitis, methemoglobinemia, bronchial asthma, and restlessness. Long term exposure: prolonged or repeated contact can cause blood damage, skin disorders, liver, kidney, and brain damage. Aminophenols may cause mutations, and there is limited teratogenic evidence. Skin allergy or asthma may develop; future exposures, even in low doses, can cause symptoms to occur. /Aminophenols/|/SIGNS AND SYMPTOMS/ o-Aminophenol is not readily absorbed through intact skin but may prove to be a sensitizing agent with resultant contact dermatitis. Inhalation of dust in excessive amounts may cause methemoglobinemia (cyanosis), irritation of mucosal membranes, and in rare instances, a bronchial asthma.|/SIGNS AND SYMPTOMS/ Inhalation of dust should be avoided because if it is inhaled in excessive amounts it may cause methemoglobinemia. In rare instances, o-aminophenol have caused a bronchial asthma.|/SIGNS AND SYMPTOMS/ Similar to ortho & para cmpd. Not readily absorbed through intact skin, but may prove to be sensitizing agent with resultant contact dermatitis. Inhalation of dust ... In excessive amt ... May cause methemoglobinemia. In rare instances o & p-aminophenol have caused bronchial asthma.|For more Human Toxicity Excerpts (Complete) data for 2-Aminophenol (7 total), please visit the HSDB record page.
2-aminophenol
The substance can be absorbed into the body by ingestion, through the skin and by inhalation of its aerosol.
See Ingestion.
MAY BE ABSORBED!
Redness.
2-Aminophenol Use and Manufacturing
The preparation method is to add o-nitrophenol and sodium sulfide into the reaction kettle, the reaction temperature is 120~125℃, the reaction time is 12h, and the stirring is continued, the reduction is completed, cooled, and acidified with hydrochloric acid to pH=6~7. Both aminophenol and sulfur are precipitated, cooled to room temperature, filtered, washed with water, and dried to obtain a crude product, and recrystallized with ethanol to obtain a finished product.
2-Aminophenol is an isomer of 4-Aminophenol (A618920) and is used as a reagent for the synthesis of heterocyclic compounds and dyes.
(1977) PROBABLY GREATER THAN 2.27X10+6 GRAMS|(1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS|Production figures for the aminophenols are scarce, the compounds usually being classified along with many other aniline derivatives. Most production of the technical grade materials (95% purity) occurs on-site as they are chiefly used as intermediate reactants in continuous chemical syntheses. World production of the fine chemicals (99% purity) is probably no more than a few hundred metric tons yearly... /Aminophenols/|Phenol, 2-amino- is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and/or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B; 51FR21438).|For more U.S. Production (Complete) data for 2-Aminophenol (6 total), please visit the HSDB record page.
Grades: technical; 99% minimum.
Phenol, 2-amino-: ACTIVE|Also available as the hydrochloride
A METHOD FOR DETECTION & IDENTIFICATION OF O-AMINOPHENOL IS PRESENTED; LIMIT OF DETECTION WAS 1-2 MUG.|HIGH-PRESSURE LIQUID CHROMATOGRAPHIC METHOD FOR DETERMINATION OF ANILINE AND ITS METABOLITES, ONE OF WHICH IS O-AMINOPHENOL, IS DISCUSSED.|PAPER CHROMATOGRAPHIC METHOD FOR SEPARATION OF ANILINE AND ITS METABOLITES, INCLUDING O-AMINOPHENOL, IS PRESENTED.|SIMULTANEOUS DETERMINATION OF AMINOPHENOL ISOMERS, INCLUDING O-AMINOPHENOL, BY HIGH-SPEED LIQUID CHROMATOGRAPHY IS REPORTED.|For more Analytic Laboratory Methods (Complete) data for 2-Aminophenol (7 total), please visit the HSDB record page.
Cosmetics -> Hair dyeing
Computed Properties
Molecular Weight:109.13
XLogP3:0.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Exact Mass:109.052763847
Monoisotopic Mass:109.052763847
Topological Polar Surface Area:46.2
Heavy Atom Count:8
Complexity:74.9
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Recommended Suppliers of 2-Aminophenol
-
CN
1 YR
Business licensedTrader Supplier of pharmaceutical intermediates,peptides,electronic chemicalsInquiryUnit Price: $33-34 /G FOBCAS No.: 95-55-6Grade: Pharmaceutical GradeContent: 99.5% -
CN
5 YRS
Business licensed Certified factoryManufactory Supplier of Active Pharm Ingredients,Chemical Catalyst,Pharmaceutical Intermediates,Flavors and Fragrances,Agrochemicals,Chemical Pesticides,Organic Intermediates,OLED IntermediatesInquiryCAS No.: 95-55-6Grade: Pharmaceutical GradeContent: 99% -
CN
5 YRS
Business licensedTrader Supplier of PVC resin,pvc paste resin,melamine -
CN
3 YRS
Business licensedTrader Supplier of CHEMICALS,REAGENTSInquiryCAS No.: 95-55-6Grade: Pharmaceutical GradeContent: 99% -
CN
3 YRS
Business licensedTrader Supplier of api,Intermediates,Organic Chemistry,Inorganic Chemistry,Daily Chemicals,Cosmetic Raw Materals,CATALYST AND AUXILIARY,FLAVORS AND FRAGRANCES,Chemical Pesticides,ADDITIVEInquiryUnit Price: $1 /KG EXWCAS No.: 95-55-6Grade: pharmaceutical gradeContent: 99%
Learn More Other Chemicals
-
2-Aminophenol glucuronide
15959-03-2
-
Disperse Violet 1
128-95-0
-
Acid Blue 1
129-17-9
-
4,5-Diamino-1-(2-hydroxyethyl)pyrazole sulfate Formula
155601-30-2
-
4-Ethoxyaniline Formula
156-43-4
-
4-(Ethylamino)phenol Formula
659-34-7
-
Phenoxazin-5-ium, 3,7-bis(diethylamino)-, chloride (1:1) Structure
33203-82-6
-
HC Blue 2 Structure
33229-34-4
-
What is Acid Red 95
33239-19-9
-
What is 7-(2H-Naphtho[1,2-d]triazol-2-yl)-3-phenyl-2H-1-benzopyran-2-one
3333-62-8