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Merck
CN

67372

标准熔点 283-286°C

analytical standard

别名:

蒽醌, ATQ

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关于此项目

经验公式(希尔记法):
C14H8O2
化学文摘社编号:
分子量:
208.21
UNSPSC Code:
20121904
NACRES:
NA.24
PubChem Substance ID:
EC Number:
201-549-0
Beilstein/REAXYS Number:
390030
MDL number:
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产品名称

标准熔点 283-286°C, analytical standard

InChI key

RZVHIXYEVGDQDX-UHFFFAOYSA-N

InChI

1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H

SMILES string

O=C1c2ccccc2C(=O)c3ccccc13

grade

analytical standard

vapor density

7.16 (vs air)

vapor pressure

1 mmHg ( 190 °C)

shelf life

limited shelf life, expiry date on the label

bp

379-381 °C (lit.)

mp

283-286 °C (±0.3°C)
284-286 °C (lit.)

application(s)

food and beverages
pharmaceutical

format

neat

Quality Level

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Application

蒽醌熔点标准品283-286℃是用于理化表征的mp标准品。
本产品还可作为热性能研究的参考标准品。

Features and Benefits

  • 可追溯至基准物质(LGC, London)的熔点校准标准品
  • 等级: 分析标准品
  • 熔点在热力学分析模式下验证
  • 标准偏差达± 0.3 °C
  • 可提供分析证书和安全数据表

General description

熔点标准温度为283-286 °C,蒽醌是一种分析标准品,适用于熔点仪的日常校准,以确保其准确性并符合地方、国家和国际标准实验室的要求。
熔点值使用基于基准物质校准的Büchi B-545设备测量,取6到12次测量的平均值。熔点采用欧洲药典(2.2.14.)所述的毛细管法测定。

pictograms

Health hazardExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Carc. 1B - Skin Sens. 1

存储类别

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

wgk

WGK 1

flash_point_f

482.0 °F - closed cup

flash_point_c

250 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Ignition mechanism of flammable dust and dust mixtures: An insight through thermogravimetric/differential scanning calorimetry analysis
Portarapillo M, et al.
AIChE Journal (2020)
Leila Qasemian et al.
Chemosphere, 84(10), 1321-1328 (2011-06-15)
Mediterranean coastal ecosystems are known to be highly subject to natural and anthropic environmental stress. In this study, we examine the effects of anthracene as a common pollutant on the total microbial communities from a Pinus halepensis litter of a
Gui'e Xie et al.
British journal of pharmacology, 159(3), 689-697 (2010-02-05)
The aims of this study were to investigate the anti-cancer activity of SZ-685C, an anthracycline analogue isolated from marine-derived mangrove endophytic fungi, and to explore the molecular mechanisms underlying such activity. The effect of SZ-685C on the viability of cancer
A A Stepanov et al.
The Journal of organic chemistry, 76(21), 8737-8748 (2011-09-14)
The nature of products in the diazotization of 1-amino-2-acetylenyl-9,10-anthraquinones strongly depends on the nature of substituents at both the alkyne and at the anthraquinone core. Donor substitution (NHAr, OH) at the fourth position stabilizes the diazonium salt at C1, decelerating
Witold Nowik et al.
Journal of chromatography. A, 1218(23), 3636-3647 (2011-05-03)
A series of reversed phases bonded with several functional groups was investigated for separation of anthraquinone derivatives, following the previous work, dedicated to the selectivity of octadecyl silica bonded phases. Considering wide diversity of substitutions in hydrophobic anthraquinone skeleton, interactions

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