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Merck
CN

36693

2-氯乙醇

PESTANAL®, analytical standard

别名:

2-氯乙基醇

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线性分子式:
ClCH2CH2OH
化学文摘社编号:
分子量:
80.51
EC Number:
203-459-7
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
878139
MDL number:
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InChI key

SZIFAVKTNFCBPC-UHFFFAOYSA-N

InChI

1S/C2H5ClO/c3-1-2-4/h4H,1-2H2

SMILES string

OCCCl

grade

analytical standard

vapor density

2.78 (vs air)

vapor pressure

5 mmHg ( 20 °C)

product line

PESTANAL®

autoignition temp.

797 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

16 %

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

refractive index

n20/D 1.441 (lit.)

bp

129 °C (lit.)

mp

−89 °C (lit.)

solubility

H2O: miscible (completely)

density

1.201 g/mL at 25 °C (lit.)

application(s)

agriculture
environmental

format

neat

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 1 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

131.0 °F - closed cup

flash_point_c

55 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Yng-Tay Chen et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 49(5), 1063-1067 (2011-01-27)
Cardiovascular effects have often been found in 2-chloroethanol (2-CE) intoxicated patients, but the 2-CE elicits cardiovascular toxicity mechanism is not clear. Recently, we have found that chloroacetaldehyde (CAA) accumulation in 2-CE-intoxicated rat's blood and play an important role in 2-CE
Mariella Carrieri et al.
Archives of toxicology, 81(7), 529-532 (2007-02-08)
Nonfatal acute inhalation of trichloroethylene (TRI) at work was described. The subject, male, 54 years old, was drawn unconscious by a metal-degreasing machine and immediately sheltered in intensive care unit. Other than basic life support and common laboratory indices, blood
Ernest Marco-Urrea et al.
Chemosphere, 70(3), 404-410 (2007-08-19)
The white-rot fungus Trametes versicolor degraded trichloroethylene (TCE), a highly oxidized chloroethene, and produced 2,2,2-trichloroethanol and carbon dioxide as the main products of degradation, based on the results obtained using [13C]-TCE as the substrate. For a range of concentrations of
John W Barton et al.
Chemosphere, 73(11), 1737-1740 (2008-10-22)
We report measurements of solubility limits for benzene, toluene, and TCE in systems that contain varying levels of biomass up to 0.13 g mL(-1) for TCE and 0.25 g mL(-1) for benzene and toluene. The solubility limit increased from 21
Edward A Lock et al.
Toxicology, 230(2-3), 234-243 (2006-12-13)
The industrial solvent trichloroethylene (TCE) and its major metabolites have been shown to cause formic aciduria in male rats. We have examined whether chloral hydrate (CH) and trichloroacetic acid (TCA), known metabolites of TCE, produce an increase in formic acid

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