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94517

Supelco

喹啉

analytical standard

别名:

1-偶氮萘, 苯并吡啶

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About This Item

经验公式（希尔记法）:
C9H7N
CAS号:
91-22-5
分子量:
129.16
Beilstein:
107477
EC號碼:
202-051-6
MDL號碼:
MFCD00006736
分類程式碼代碼:
85151701
PubChem物質ID:
329770348
NACRES:
NA.24

等級

analytical standard

品質等級

100

蒸汽密度

4.5 (vs air)

蒸汽壓力

0.07 mmHg ( 20 °C)

化驗

≥98.0% (GC)
97.5-102.2% (wt., NT)

自燃溫度

896 °F

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.625 (lit.)

bp

113-114 °C/11 mmHg (lit.)
237 °C (lit.)

mp

−17-−13 °C (lit.)

密度

1.093 g/mL at 25 °C (lit.)

應用

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

格式

neat

SMILES 字串

c1ccc2ncccc2c1

InChI

1S/C9H7N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-7H

InChI 密鑰

SMWDFEZZVXVKRB-UHFFFAOYSA-N

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訊號詞

Danger

危險分類

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Chronic 2 - Carc. 1B - Eye Irrit. 2 - Muta. 2 - Skin Irrit. 2

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類（WGK）

WGK 2

閃點（°F）

213.8 °F - closed cup

閃點（°C）

101 °C - closed cup

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分析证书(COA)

Lot/Batch Number
BCCL9303
BCCG1563
BCBX3571
BCBT7647
BCBM6682V

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Current medicinal chemistry, 17(18), 1960-1973 (2010-04-10)
Although the assortment of antifungal drugs is broad, the most commonly used agents have major drawbacks. Toxicity, serious side effects or the emergence of drug resistance are amongst them. New drugs and drug candidates under clinical trials do not guarantee
Alexander P Gorka et al.
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Historically, the most successful molecular target for antimalarial drugs has been heme biomineralization within the malarial parasite digestive vacuole. Heme released from catabolized host red blood cell hemoglobin is toxic, so malarial parasites crystallize heme to nontoxic hemozoin. For years
Chunrong Wang et al.
Bioscience, biotechnology, and biochemistry, 79(1), 164-170 (2014-09-02)
A novel quinoline-degrading strain, named K4, was isolated from activated sludge of a coking wastewater treatment plant and identified as Brevundimonas sp. on the basis of its 16s rDNA gene sequence analysis. Its optimum temperature and pH for quinoline degradation
Paul D Roepe
Future microbiology, 4(4), 441-455 (2009-05-07)
30 years before the discovery of the pfcrt gene, altered cellular drug accumulation in drug-resistant malarial parasites had been well documented. Heme released from catabolized hemoglobin was thought to be a key target for quinoline drugs, and additional modifications to
Mohanad Darawsheh et al.
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Starting from the precursor [Zinc Valproate complex] (1), new mixed ligand zinc(II) complexes of valproic acid and nitrogen-based ligands, formulating as, [Zn(valp)22,9-dmphen] (2), [Zn2(valp)4(quin)2] (3), [Zn(valp)2(2-ampy)2] (4), and [Zn(valp)2(2-ampic)2] (5) (valp = valproate, 2,9-dmphen = 2,9-dimethyl-1,10-phenanthroline, quin = quinoline, 2-ampy
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