79356-06-2

Basic information

• Product Name: 1,2,3,4-tetrahydrochrysene-1,2,3,4-tetrol
• Synonyms: 1,2,3,4-Chrysenetetrol, 1,2,3,4-tetrahydro-
• CAS NO: 79356-06-2
• Molecular Formula: C₁₈H₁₆O₄
• Molecular Weight: 296.3172
• Mol File: 79356-06-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 563°C at 760 mmHg
• Flash Point: 272.8°C
• Density: 1.539g/cm³
• Vapor Pressure: 1.64E-13mmHg at 25°C
• Refractive Index: 1.837
• CAS DataBase Reference: 1,2,3,4-tetrahydrochrysene-1,2,3,4-tetrol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4-tetrahydrochrysene-1,2,3,4-tetrol(79356-06-2)
• EPA Substance Registry System: 1,2,3,4-tetrahydrochrysene-1,2,3,4-tetrol(79356-06-2)

Safety Data

• Hazardous Substances Data: 79356-06-2(Hazardous Substances Data)

Upstream product

• 64920-33-8 trans-1,2-dihydroxy-anti-3,4-epoxy-1,2,3,4-tetrahydrochrysene 

Relevant articles and documents

Detection of DNA and globin adducts of polynuclear aromatic hydrocarbon diol epoxides by gas chromatography - Mass spectrometry and [3H]CH3I postlabeling of released tetraols

Gas chromatography - negative ion chemical ionization mass spectrometry - selected ion monitoring (GC-NICI-MS-SIM) was employed to detect tetramethyl ether derivatives of tetraols formed upon hydrolysis of DNA and globin adducts derived from diol epoxides of benzo[α]-pyrene (BP) and other polynuclear aromatic hydrocarbons (PAH). The tetramethyl ether derivatives could also be detected by [3H]CH3I postlabeling. The methodology involves the following steps: (1) isolation of DNA or globin; (2) mild acid hydrolysis under vacuum; (3) isolation of the resulting tetraols and derivatization to the corresponding tetramethyl ethers using methyl sulfinyl carbanion and unlabeled or 3H-labeled CH3I; (4) analysis by GC-NICI-MS-SIM or HPLC with radioflow detection. The optimum conditions for hydrolysis of adducts and derivatization of the resulting tetraols as well as the feasibility of this approach for detecting PAH adducts in mice and humans were explored. Using the set of four BP-tetraols that can be formed upon hydrolysis of adducts formed from r-7,t-8-dihydroxy-t-9,10-epoxy-7,8,9,10-tetrahydrobenzo[α]pyrene (anti-BPDE) or r-7,t-8-dihydroxy-c-9,10-epoxy-7,8,9,10-tetrahydrobenzo-[α]pyrene (syn-BPDE) as models, the stability of the tetraols under the hydrolysis conditions was investigated. Adducts derived from anti-BPDE yield predominantly the stable r-7,t-8,9-c-10-tetrahydroxy-7,8,9,10-tetrahydrobenzo[α]pyrene (trans-anti-BP-tetraol), while adducts derived from syn-BPDE released cis-syn-BP-tetraol as a major hydrolysis product. Hydrolysis under vacuum significantly increased the recovery of tetraols. Conditions for derivatization of the BP-tetraols as well as tetraols derived from several other PAH anti-diol epoxides were investigated. Tetramethyl ethers proved to be superior derivatives that were stable, easy to prepare in high yields, and detectable with high sensitivity by GC-NICI-MS-SIM (1-50 fmol per injection). Alternatively, these derivatives could be detected by HPLC with radioflow detection if [3H]CH3I were employed for derivatization. The methodology was tested by comparing levels of DNA and globin adducts in mice treated with either unlabeled or 3H-labeled BP. Good agreement was obtained among the GC-NICI-MS-SIM, [3H]CH3I postlabeling, and conventional radiometric methods. Moreover, analysis of human hemoglobin by GC-NICI-MS-SIM resulted in detection of adducts derived from anti-BPDE and r-1,t-2-dihydroxy-t-3,4-epoxy-1,2,3,4-tetrahydrochrysene. The results of this study demonstrate that GC-NICI-MS-SIM of tetramethyl ethers of tetraols formed by hydrolysis of PAH diol epoxide DNA and globin adducts is a promising approach for detection and quantitation of adducts derived from a broad range of PAH.