1,2-Benzoldicarboxaldehyd

Phthalaldehyde

HCID 4807CAS 643-79-8

Grundinformationen

Standard-SMILES
O=Cc1ccccc1C=O
InChIKey
ZWLUXSQADUDCSB-UHFFFAOYSA-N
Summenformel
C8H6O2
Durchschnittliche Molmasse
134,13 g/mol
Monoisotopische Masse
134,03677943

Überblick

Phthalaldehyde is a dialdehyde in which two formyl groups are attached to adjacent carbon centres on a benzene ring. It has a role as an epitope. It is a member of benzaldehydes and a dialdehyde.

Namen und Bezeichner

Bevorzugter Name
Phthalaldehyde
IUPAC
phthalaldehyde
Lokaler Name
1,2-Benzoldicarboxaldehyd
Englischer Name
o-Phthalaldehyde
Summenformel
C8H6O2
Molmasse
134.13

Namen und Synonyme

o-Phthalaldehyde643-79-8PHTHALALDEHYDEo-Phthaldialdehyde1,2-BenzenedicarboxaldehydePhthalic aldehydeortho-Phthalaldehydebenzene-1,2-dicarbaldehydePhthalic dialdehydePhthalic dicarboxaldehydePhthalyldicarboxaldehydePhthalaldialdehyde
Weitere Namen anzeigen
OPAOPDPHTHALDIALDEHYDEO-PHTHALDEHYDE1,2-PHTHALIC DICARBOXALDEHYDEPhthaldialdehy
ortho Phthalaldehydeo-Phthalicdicarboxaldehyde1,2-DiformylbenzenephtharalPhtalaldehydesDisopaDTXSID6032514CHEBI:70851

Datenbank-Bezeichner

CAS
643-79-8
PubChem CID
4807
DTXSID
DTXSID6032514
ChEMBL
CHEMBL160145
ChEBI
CHEBI:70851
UNII
4P8QP9768A
EC Number
211-402-2
Nikkaji
J45.641A

Eigenschaften

Berechnete Struktureigenschaften

XLogP
1,2
Polarare Oberfläche (TPSA)
34,1 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
2
Frei drehbare Bindungen
2
Schwere Atome
10

Experimentelle und physikochemische Eigenschaften

Chemical ClassesOther Classes -> Benzaldehydes
SpringerMaterials PropertiesCrystal structure
PesticidesEnvironmental transformation -> Pesticide transformation products (metabolite, successor)
LogP · 2 Einträge

log Kow = 0.51

0.99 (30 °C)

DensityDensity (at 20 °C): 1.13 g/cm³
Color/Form · 2 Einträge

Long, pale yellow needles from petroleum ether (MP 56-56.5 °C). Also reported as colorless powder (MP: 54 °C)

Yellow needles or crystals from ligroin

Physikochemische Eigenschaften

Schmelzpunkt
55 · 55-58 °C(lit.)
Siedepunkt
83 · 83-84 °C (0.7501 mmHg)
Dichte
1.13 · 1.13
Dampfdruck
0.56 Pa · 0.56Pa at 25℃
Brechungsindex
1.45 · 1.4500 (estimate)
Flammpunkt
230 °F · >230 °F

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H228 (44.3%): Flammable solid [Danger Flammable solids]

P210, P240, P241, P260, P261, P264, P264+P265, P270, P271, P272, P273, P280, P301+P316, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P319, P321, P330, P332+P317, P333+P317, P362+P364, P363, P370+P378, P391, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 235 reports by companies from 15 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Danger

H301: Toxic if swallowed [Danger Acute toxicity, oral]

Gefahrenhinweise

Regulatory Information · 3 Einträge

Chemical: 1,2-Benzenedicarboxaldehyde

Status: Active Update: 19-02-2019 https://echa.europa.eu/registration-dossier/-/registered-dossier/27723

Phthaldialdehyde: Does not have an individual approval but may be used under an appropriate group standard

Fire HazardsCombustible.
Hazards Summary · 1 Eintrag

Similar properties and health effects to glutaraldehyde; [ACGIH] Severe gastrointestinal tract damage and hematological changes observed in 90-day oral study of rats; Delayed skeletal development observed in rats at doses maternally toxic; [NTP] Symptoms reported from occupational exposure to Cidex-OPA (aqueous solution containing 0.56% o-phthalaldehyde) include exacerbation of asthma, anaphylaxis, burns and/or irritation, and dermal hypersensitivity; [NTP] Causes burns; Inhalation may cause corrosive injuries to upper respiratory tract and lungs; May cause skin sensitization; Toxic by ingestion; [Alfa Aesar MSDS] Occupational asthma confirmed in an endoscopy unit worker; [Malo] See Benzaldehyde. See 2-Methylbenzaldehyde.

UN ClassificationUN Hazard Class: 8; UN Subsidiary Risks: 6.1; UN Pack Group: II
Chemical DangersReacts with oxidants, amines and strong bases. This generates fire and explosion hazard.
Packaging and LabellingDo not transport with food and feedstuffs. Marine pollutant.

Sicherheit und Schutzausrüstung

Fire FightingUse carbon dioxide, dry powder, foam, water.
First Aid Measures · 4 Einträge

Fresh air, rest. Artificial respiration may be needed. Refer immediately for medical attention.

Wear protective gloves when administering first aid. Remove contaminated clothes. Rinse skin with plenty of water or shower for at least 15 minutes. Refer immediately for medical attention.

Rinse with plenty of water for several minutes (remove contact lenses if easily possible). Refer immediately for medical attention.

Rinse mouth. Do NOT induce vomiting. Refer immediately for medical attention.

Safe StorageWell closed. Separated from oxidants, amines, strong bases and food and feedstuffs. Ventilation along the floor. Store in an area without drain or sewer access. Provision to contain effluent from fire extinguishing.
Fire Fighting Procedures · 2 Einträge

Suitable extinguishing media: Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.

Advice for firefighters: Wear self-contained breathing apparatus for firefighting if necessary.

Storage Conditions · 1 Eintrag

Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature 2-8 °C. Light sensitive. Moisture sensitive. Store under inert gas. Keep in a dry place. Storage class (TRGS 510): Non-combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials.

Cleanup Methods · 1 Eintrag

ACCIDENTAL RELEASE MEASURES: Personal precautions, protective equipment and emergency procedures: Wear respiratory protection. Avoid dust formation. Avoid breathing vapors, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. Environmental precautions: Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Discharge into the environment must be avoided. Methods and materials for containment and cleaning up: Pick up and arrange disposal without creating dust. Sweep up and shovel. Keep in suitable, closed containers for disposal.

Toxikologische Informationen

Ecotoxicity Values · 5 Einträge

LD50; Species: Anas platyrhychos (Mallard duck) age 18 weeks; oral via capsule 738 mg/kg (95% confidence interval: 390-1763 mg/kg) /99% purity/

EC50; Species: Pseudokirchneriella subcapitata (Green algae); Conditions: freshwater, static; Concentration: 0.22 mg/L for 96 hr; Effect: popuation abundance /formulatilon/

EC50; Species: Pseudokirchneriella subcapitata (Green algae); Conditions: freshwater, static; Concentration: 0.184 mg/L for 96 hr (95% confidence interval: 0.171-0.2 mg/L); Effect: popuation abundance /98% purity/

EC50; Species: Daphnia magna (Water flea) age <24 hr; Conditions: freshwater, static; Concentration: 0.09 mg/L for 48 hr (95% confidence interval: 0.08-0.12 mg/L); Effect: intoxication, immobilization /99.6% purity/

For more Ecotoxicity Values (Complete) data for o-Phthalaldehyde (6 total), please visit the HSDB record page.

Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 10(SRC), determined from a structure estimation method(2), indicates that o-phthalaldehyde is expected to have very high mobility in soil(SRC). Volatilization of o-phthalaldehyde from moist soil surfaces is not expected(SRC) given an estimated Henry's Law constant of 1.8X10-8 atm-cu m/mole(SRC) based upon its vapor pressure, 5.2X10-3 mm Hg(3), and water solubility, 5.0X10+4 mg/L(3). o-Phthalaldehyde is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(3). Biodegradation data in soil were not available(SRC, 2018).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 10(SRC), determined from a structure estimation method(2), indicates that o-phthalaldehyde is not 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 1.8X10-8 atm-cu m/mole(SRC), derived from its vapor pressure, 5.2X10-3 mm Hg(4), and water solubility, 5.0X10+4 mg/L(4). o-Phthalaldehyde is not expected to undergo hydrolysis in the environment due to the lack of functional groups that hydrolyze under environmental conditions(3). According to a classification scheme(5), an estimated BCF of 3(SRC), from a log Kow of 0.51(4) and a regression-derived equation(2), suggests the potential for bioconcentration in aquatic organisms is low. Biodegradation data in water were not available(SRC, 2018).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), o-phthalaldehyde, which has a vapor pressure of 5.2X10-3 mm Hg at 21 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase o-phthalaldehyde 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 17 hours(SRC), calculated from its rate constant of 2.3X10-11 cu cm/molecule-sec at 25 °C(3). o-Phthalaldehyde has an absorption peak at 297 nm(3) and, therefore, may be susceptible to direct photolysis by sunlight(SRC).

Adverse EffectsDermatotoxin - Skin burns.
Exposure RoutesSerious local effects on contact with eyes and skin. The substance can be absorbed into the body by inhalation of its vapour or dust and by ingestion.
Toxicity Summary · 1 Eintrag

IDENTIFICATION AND USE: o-Phthalaldehyde (OPA) is used as disinfectant and reagent in fluorometric determination of primary amines and thiols. HUMAN STUDIES: OPA is a commonly used solution for rapid sterilization of medical equipment. Cases of anaphylaxis following cystoscopy with endoscopes sterilized with this agent have been reported. OPA-induced anaphylaxis following laryngoscopy have also been described. In these patients, OPA-specific IgE was detected in the serum. Contact dermatitis occurred in 4 workers of the endoscopy unit, one of whom also developed asthma. Among 80 female disinfection workers who used only antiseptic solutions containing OPA, the incidence of disinfection-related complaints were 10% skin, 9% eye, and 16% respiratory symptoms. ANIMAL STUDIES: In male mice, injected OPA induced specific IgE and IgG in the sera, suggesting that OPA acts as a hapten. Overall, OPA caused acute inflammation and acted as a haptenic allergen, although it caused only mild liver injury. In mice sensitized to ovalbumin (OVA), OPA enhanced the OVA-induced recruitment of neutrophils to the lung and the production of allergen-specific IgE, suggesting that OPA acts as an immunological adjuvant. The major targets from OPA exposure in rats and mice included the respiratory system (nasal cavity, larynx, trachea, and lung), skin, eye, testis, and epididymis. The most sensitive measure of OPA inhalation toxicity in male and female rats and mice was significantly increased incidences of nasal cavity lesions (lowest-observable-effect concentration = 0.44 ppm). OPA was mutagenic in Salmonella typhimurium strain TA100 in the absence of exogenous metabolic activation; no mutagenicity was seen in TA100 with metabolic activation or in TA98 or Escherichia coli WP2 uvrA/pKM101, with or without metabolic activation.

Signs and Symptoms · 4 Einträge

Cough. Shortness of breath. Headache.

Redness. Pain. Serious skin burns.

Redness. Pain. Severe burns.

Burns in mouth and throat. Nausea. Diarrhoea. Vomiting.

Sicherheitsdaten

F
1-8-10
wgk
3
tsca
TSCA listed
ridadr
UN2923 8/PG 2
hs_code
29122900
RTECS-Nr.
TH6950000

Chemie und Industrie

Pharmakologische Informationen

MeSH Pharmacological Classification · 3 Einträge

Substances used on inanimate objects that destroy harmful microorganisms or inhibit their activity. Disinfectants are classed as complete, destroying SPORES as well as vegetative forms of microorganisms, or incomplete, destroying only vegetative forms of the organisms. They are distinguished from ANTISEPTICS, which are local anti-infective agents used on humans and other animals. (From Hawley&apos;s Condensed Chemical Dictionary, 11th ed)

Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction.

Substances used for the detection, identification, analysis, etc. of chemical, biological, or pathologic processes or conditions. Indicators are substances that change in physical appearance, e.g., color, at or approaching the endpoint of a chemical titration, e.g., on the passage between acidity and alkalinity. Reagents are substances used for the detection or determination of another substance by chemical or microscopical means, especially analysis. Types of reagents are precipitants, solvents, oxidizers, reducers, fluxes, and colorimetric reagents. (From Grant &amp; Hackh&apos;s Chemical Dictionary, 5th ed, p301, p499)

Verwendung und Herstellung

Uses · 6 Einträge

Used as a disinfectant and in the fluorometric determination of primary amines and thiols; [Merck Index] Used to sterilize medical and dental equipment, as an enzyme inhibitor, indicator, chemical intermediate, diagnostic agent, tanning agent for leather, in water treatment, pulp and paper manufacturing, oil field water flooding, hair colorings, wood treatment, and antifouling paints; [NTP]

Petroleum Production and Refining [Category: Industry]

For o-phthalaldehyde (USEPA/OPP Pesticide Code: 129017) there are 0 labels match. /SRP: Not registered for current use in the USA, but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./

Reagents used to synthesize fluorescent derivatives for chemical analyses: Derivatized compound: primary amines. /From table/

Disinfectant. Reagent in fluorometric determination of primary amines and thiols.

/o-Phthalaldehyde/ ... in conjunction with 2-mercaptoethanol, is most often used in post-column detection of amino acids separated by conventional automated amino acid analysis.

Use ClassificationEnvironmental transformation -> Pesticide transformation products (metabolite, successor)
General Manufacturing Information1,2-Benzenedicarboxaldehyde: ACTIVE

Anwendungen

Verwendeno-Phthalaldehyde can be widely used for precolumn derivatization of amino acids in HPLC separation or Capillary electrophoresis. For flow cytometric measurements of protein thiol groups.

Darstellung · 1 Eintrag

synthetischeo-Phthalaldehyde is a high-level chemical disinfectant that is commonly used for disinfection of dental and medical instruments as an alternative to glutaraldehyde, which is a known skin and respiratory sensitizer. A variety of processes for manufacturing o-phthalaldehyde have been reported in the literature. o-Phthalaldehyde is produced by heating pure benzaldehyde and chloroform with potassium hydroxide solution. The resulting solution is further acidified with hydrochloric acid and cooled to yield a colorless powder of o-phthalaldehyde. It is also produced by ozonization of naphthalene in alcohol followed by catalytic hydrogenation. Catalytic oxidation of various chemicals is also used in manufacturing o-phthalaldehyde. o-Phthalaldehyde can be manufactured by oxidation of phthalan by nitrogen monoxide in acetonitrile with N-hydroxyphthalimide as the catalyst to yield 80% to 90%.

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Ergänzende Hinweise · 2 Einträge

DefinitionUsing o-phthalaldehyde (OPA) in combination with a thiol reagent is a standard method for detecting primary amines in amino acids, peptides, and proteins. O-phthalaldehyde, in the presence of 2-mercaptoethanol, reacts with primary amines to form highly fluorescent products. Picomole quantities of amino acids, peptides, and proteins can be detected easily. o-Phthalaldehyde is five to ten times more sensitive than fluorescamine and is soluble and stable in aqueous buffers. Despite its widespread use, the exact reaction mechanism has been debated since the 1980s. Rovelli's results support the mechanism originally proposed by Sternson and Wong, in which the primary amine first reacts with OPA, followed by a reaction with the thiol to form the fluorescent isoindole product[1-2].

DefinitionChEBI: A dialdehyde in which two formyl groups are attached to adjacent carbon centres on a benzene ring.

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