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Merck
CN

03378

氯化物标准浓缩液 10.00g Cl-

10.00 g/L, for 1 l standard solution, analytical standard

别名:

盐酸 溶液, 氯化氢 溶液

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关于此项目

经验公式(希尔记法):
HCl
化学文摘社编号:
分子量:
36.46
UNSPSC Code:
41116107
PubChem Substance ID:
MDL number:
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grade

analytical standard

vapor pressure

190 mmHg ( 25 °C)

shelf life

limited shelf life, expiry date on the label

packaging

ampule of

concentration

10.00 g/L

bp

100 °C (lit.)

solubility

H2O: soluble

format

single component solution

SMILES string

Cl

InChI

1S/ClH/h1H

InChI key

VEXZGXHMUGYJMC-UHFFFAOYSA-N

General description

This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

Preparation Note

用 HCl 和 H2O 制备


pictograms

Corrosion

signalword

Warning

hcodes

Hazard Classifications

Met. Corr. 1

存储类别

8B - Non-combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

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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Jay G Hosking et al.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 40(4), 1005-1015 (2014-10-21)
Successful decision making often requires weighing a given option's costs against its associated benefits, an ability that appears perturbed in virtually every severe mental illness. Animal models of such cost/benefit decision making overwhelmingly implicate mesolimbic dopamine in our willingness to
Ann Brinkmalm et al.
Molecular neurodegeneration, 9, 53-53 (2014-11-25)
Synaptic degeneration is an early pathogenic event in Alzheimer's disease, associated with cognitive impairment and disease progression. Cerebrospinal fluid biomarkers reflecting synaptic integrity would be highly valuable tools to monitor synaptic degeneration directly in patients. We previously showed that synaptic
Sandra Donkervoort et al.
Human mutation, 36(1), 48-56 (2014-09-11)
Collagen 6-related dystrophies and myopathies (COL6-RD) are a group of disorders that form a wide phenotypic spectrum, ranging from severe Ullrich congenital muscular dystrophy, intermediate phenotypes, to the milder Bethlem myopathy. Both inter- and intrafamilial variable expressivity are commonly observed.



全球贸易项目编号

货号GTIN
128376-10G04061838725523
818537002504022536438689
128376-50G04061838725547
128376-250G04061838725530