o-Phthalaldehyde

o-Phthalaldehyde
  • CAS No.:643-79-8
Other grades of this product :
o-Phthalaldehyde Basic information
Product Name:o-Phthalaldehyde
Synonyms:The developMent of forMaldehyde;O-PHTHALDIALDEHYDE REAGENT SOLUTION*;PHTHALALDEHYDE;TIMTEC-BB SBB008450;2-PHTHALALDEHYDE;2-PHTHALDEHYDE;2-PHTHALDIALDEHYDE;o-Phenyldialdehyde
CAS:643-79-8
MF:C8H6O2
MW:134.13
EINECS:211-402-2
Product Categories:marker;Derivatization Reagents TLC;Detection Products for Amino Acid Analysis;Fluorescent Labels;Functional Group Reactive Label;Functional Group Reactive Labels;Aldehydes;Alphabetical;Amino Acids;Analytical Reagents;Analytical/Chromatography;Application Specific Reagents;Biochemicals and Reagents;Building Blocks;C8;Chemical Synthesis;Derivatization Reagents;Derivatization Reagents HPLC;Detection;Electrochemical;Fluorescence;Fluorescent Indicators and Probes;Fluorescent Probes;Labels;Particles and Stains;Peptide Analysis and Characterization;Carbohydrates;Core Bioreagents;Functional Group Reactive Labels for Flow Cytometry;Organic Building Blocks;Carbonyl Compounds;Amino Group Labeling Reagents for Fluorescence HPLC;Amino Group Labeling Reagents for HPLC;Analytical Chemistry;Fluorescence Detection (HPLC Labeling Reagents);HPLC Labeling Reagents;UV Detection (HPLC Labeling Reagents);Amino Acid Analysis;Carbohydrate Labels;Carbohydrate Labels for Chromatography;Peptides;Research Essentials;Analytical Reagents for General Use;by Application;Derivatization agents;HPLC Derivatization Reagents;Luminescent Compounds/Detection;O-P;Puriss p.a.;Thiols;643-79-8;bc0001
Mol File:643-79-8.mol
o-Phthalaldehyde Chemical Properties
Melting point 55-58 °C(lit.)
Boiling point 83-84 °C (0.7501 mmHg)
density 1.13
vapor pressure 0.56Pa at 25℃
refractive index 1.4500 (estimate)
Fp >230 °F
storage temp. 2-8°C
solubility The solubility of o-phthalaldehyde is 3g/100 mL diisopropyl ether, 5g/100mL deionized water, 20g/100mL chloroform, or 20g/100mL acetone at 20°C.
form powder
color yellow
PH7 (53g/l, H2O, 20℃)
Water Solubility soluble
Sensitive Air Sensitive
Merck 14,7368
BRN 878317
Exposure limitsACGIH: SL .025 mg/100 cm2; Ceiling 0.1 ppb (Skin)
Stability:Stable. Air sensitive. Incompatible with strong oxidizing agents, strong bases.
InChIKeyZWLUXSQADUDCSB-UHFFFAOYSA-N
LogP0.99 at 30℃
CAS DataBase Reference643-79-8(CAS DataBase Reference)
NIST Chemistry ReferenceO-phthalaldehyde(643-79-8)
EPA Substance Registry System1,2-Benzenedicarboxaldehyde (643-79-8)
Safety Information
Hazard Codes Xi,T,N,C
Risk Statements 36/37/38-43-34-25-50-52/53
Safety Statements 26-28-36-45-36/37/39-61-37/39
RIDADR UN2923 8/PG 2
WGK Germany 3
RTECS TH6950000
1-8-10
Autoignition Temperature480 °C
Hazard Note Irritant/Air Sensitive
TSCA Yes
HazardClass 8
PackingGroup 
HS Code 29122900
Hazardous Substances Data643-79-8(Hazardous Substances Data)
ToxicityLD50 orally in Rabbit: 178 mg/kg LD50 dermal Rat > 2000 mg/kg
MSDS Information
ProviderLanguage
1,2-Phthalic dicarboxaldehyde English
SigmaAldrich English
ACROS English
ALFA English
o-Phthalaldehyde Usage And Synthesis
Chemical Propertieso-Phthalaldehyde is a pale yellow crystalline solid. o-Phthalaldehyde is mainly used as a high-level disinfectant (a low-temperature chemical method) for heat-sensitive medical and dental equipment such as endoscopes and thermometers; in recent years, it has gained popularity as a safe and better alternative to glutaraldehyde. There are some researches show, pH7.5 contains the sterilizing agent of o-phthalaldehyde 0.5%, and its sterilizing power, sterilization speed, stability and toxicity all are better than glutaraldehyde, can kill mycobacterium in the 5min, the bacterium number reduces by 5 logarithmic value, and o-phthalaldehyde is very stable, tasteless in pH3~9 scopes, non-stimulated to human nose, eye mucosa, and need not activate before using, various materials are had good consistency, have tangible microbiocidal activity.
Useso-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.
Useso-Phthalaldehyde can be used for precolumn derivatization of amino acids for HPLC separation and for flow cytometric measurements of protein thiol groups.
UsesPrecolumn derivatization reagent for primary amines and amino acids. The fluorescent derivative can be detected by reverse-phase HPLC. The reaction requires OPA, primary amine and a sulfhydryl. In the presence of excess sulfhydryl, amines can be quantitated. In the presence of excess amine, sulfhydryls can be quantitated.
UsesDisinfectant. Reagent in fluorometric determination of primary amines and thiols.
Preparationo-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%.
DefinitionChEBI: A dialdehyde in which two formyl groups are attached to adjacent carbon centres on a benzene ring.
Synthesis Reference(s)Journal of the American Chemical Society, 73, p. 1668, 1951 DOI: 10.1021/ja01148a076Tetrahedron Letters, 27, p. 1793, 1986 DOI: 10.1016/S0040-4039(00)84377-4
Flammability and ExplosibilityNotclassified
Biotechnological ApplicationsO-phthalaldehyde(OPA) is used for precolumn derivatization of amino acids for HPLC separation and for flow cytometric measurements of protein thiol groups. Used for fluorometric determination of histamine, histidine and other amino acids. Also used for cholesterol assay in the picomole range. Phthaldialdehyde has been used: in the preparation of O-phthaldialdehyde reagent for analysing gentamycin content. in the preparation of reagent for determining the degree of hydrolysis of milk proteins. in the measurement of free amino acids of milk samples by O-phthaldialdehyde/N-acetyl-L-cysteine (OPA/NAC) assay. in the derivatization of putrescine samples.
Potential ExposureThe primary routes of human exposure to o-phthalaldehyde are by inhalation and through the skin, which may occur through accidental or occupational exposures. Along with its increasing popularity as a chemical sterilizer, o-phthalaldehyde has many applications in analytical methods and in diagnostic kits. o-Phthalaldehyde is also used as an intermediate in the synthesis of pharmaceuticals and as a reagent in the tanning industry, hair colorings, wood treatment, and antifouling paints. o-Phthalaldehyde was approved for use as an indoor antimicrobial pesticide in 1997; however, it is no longer registered with the United States Environmental Protection Agency (USEPA) for this use.
CarcinogenicityNo information on the carcinogenicity of o-phthalaldehyde in experimental animals or humans was found in a review of the literature.

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