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2-Aminofluorene structure, CAS 153-78-6

2-Aminofluorene

CAS Number153-78-6

Synonyms9H-Fluoren-2-amine; EINECS 205-817-8; 2-aminofluorene; 2-Amino fluorene; 9H-Fluoren-2-ylamine; MFCD00001125; 2-Fluorenamine

Molecular FormulaC13H11N

Molecular Weight181.23

Purity98%

Density1.2±0.1 g/cm3

Boiling Point379.3±21.0 °C at 760 mmHg

Melting Point124-128 °C (lit.)

Flash Point

Appearancepowder

EINECS205-817-8

MSDSChineseEnglish

Symbol6.1

Signal WordWarning

Cat. No.: 2A-9002452 Purity: 98%
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Quality Control of [ 153-78-6 ] Purity: 98% SDS Specification MoL

COA NMR CNMR HPLC LC-MS
Chemical & Physical Properties
CAS Number153-78-6
Catalog No.2A-9002452
Chinese Name2-氨基芴
Synonyms9H-Fluoren-2-amine; EINECS 205-817-8; 2-aminofluorene; 2-Amino fluorene; 9H-Fluoren-2-ylamine; MFCD00001125; 2-Fluorenamine
Molecular FormulaC13H11N
Molecular Weight181.23
Purity98
Density1.2±0.1 g/cm3
Boiling Point379.3±21.0 °C at 760 mmHg
Melting Point124-128 °C (lit.)
Appearancepowder
Water Solubility<0.1 g/100 mL at 19.5 ºC
Storage ConditionShould be kept sealed.
PackagingI; II; III
Application2-Aminofluorene is a synthetic chemical pesticide. 2-Aminofluorene is a genotoxin. 2-Aminofluorene can be used to study DNA adduct structure, DNA repair, carcinogenesis and mutagenesis [1][4].
EINECS205-817-8
HTC29214980
PubChem ID24890992
MDL NumberMFCD00001125
SMILESNc1ccc-2c(Cc3ccccc-23)c1
InChI1S/C13H11N/c14-11-5-6-13-10(8-11)7-9-3-1-2-4-12(9)13/h1-6,8H,7,14H2
InChI KeyCFRFHWQYWJMEJN-UHFFFAOYSA-N
Beilstein/REAXYS1945861
NACRES CodeNA.22
UNSPSC12352100
Hazard Symbols6.1
Risk CodesR40;R68
Safety DescriptionS36/37;S45
MSDSmsds/2452_1_153_78_6.pdf
Bioactivity2-Aminofluorene is a synthetic chemical insecticide. 2-Aminofluorene is a genotoxin. 2-Aminofluorene can be used in the research of DNA adduct structure, DNA repair, carcinogenesis, and mutagenesis[1][4]. Related Catalog Signaling Pathways >> Cell Cycle/DNA Damage >> DNA/RNA Synthesis Research Areas >> Others In Vitro 2-Aminofluorene (0-100 μM, 1-5 days) produces a dose-related suppression of the antibody response to sheep erythrocytes (SRBC), DNP-Ficoll, and LPS[2]. 2-Aminofluorene (0-100 μM, 3 days, spleen cells) produces suppression on lymphoproliferative responses to LPS and Con A[2]. In Vivo 2-Aminofluorene (60 mg/kg, i.p.) accumulates twice the 2-Aminofluorene-DNA adducts of slow acetylators (A/J) in rapid acetylator mice (C57BL/6J)[3]. 2-Aminofluorene (60 mg/kg, i.p.) forms significantly higher levels of DNA adducts in tumor-target organs than in non-target organs in acetylator congenic hamsters[4]. References [1]. Heflich RH, et al. Genetic toxicity of 2-acetylaminofluorene, 2-aminofluorene and some of their metabolites and model metabolites. Mutat Res. 1994 Oct;318(2):73-114. [2]. Kim BS, et al. Immunosuppressive effects of 2-acetylaminofluorene and 2-aminofluorene on murine splenocytes culture. Drug Chem Toxicol. 1989 Sep-Dec;12(3-4):297-311. [3]. Levy GN, et al. 2-Aminofluorene-DNA adduct formation in acetylator congenic mouse lines. Carcinogenesis. 1989 Apr;10(4):705-9. Chemical & Physical Properties Density 1.2±0.1 g/cm3 Boiling Point 379.3±21.0 °C at 760 mmHg Melting Point 124-128 °C(lit.) Molecular Formula C13H11N Molecular Weight 181.233 Flash Point 204.8±17.4 °C Exact Mass 181.089142 PSA 26.02000 LogP 2.88 Vapour Pressure 0.0±0.9 mmHg at 25°C Index of Refraction 1.697 Water Solubility <0.1 g/100 mL at 19.5 ºC
Use ofProperties Articles34 Name 2-Aminofluorene Synonym More Synonyms 2-aminofluorene Biological Activity Related Catalog Signaling Pathways >> Cell Cycle/DNA Damage >> DNA/RNA Synthesis Research Areas >> Others In Vitro 2-Aminofluorene (0-100 μM, 1-5 days) produces a dose-related suppression of the antibody response to sheep erythrocytes (SRBC), DNP-Ficoll, and LPS[2]. 2-Aminofluorene (0-100 μM, 3 days, spleen cells) produces suppression on lymphoproliferative responses to LPS and Con A[2]. References [1]. Heflich RH, et al. Genetic toxicity of 2-acetylaminofluorene, 2-aminofluorene and some of their metabolites and model metabolites. Mutat Res. 1994 Oct;318(2):73-114. [2]. Kim BS, et al. Immunosuppressive effects of 2-acetylaminofluorene and 2-aminofluorene on murine splenocytes culture. Drug Chem Toxicol. 1989 Sep-Dec;12(3-4):297-311. [3]. Levy GN, et al. 2-Aminofluorene-DNA adduct formation in acetylator congenic mouse lines. Carcinogenesis. 1989 Apr;10(4):705-9. Chemical & Physical Properties Molecular Formula C13H11N Exact Mass 181.089142 PSA 26.02000 Index of Refraction 1.697
Transport InfoProduct name: Purity: 98.0%
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available The above information is believed to be correct, but is not all-inclusive and should be used as a guide only. The information in this document is based on our current knowledge and is Correct safety instructions apply to this product. This information does not represent a warranty as to the properties of this product. See reverse side of invoice or packing slip.
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