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BP567

卡替洛尔 盐酸盐

British Pharmacopoeia (BP) Reference Standard

别名:

Carteolol monohydrochloride

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关于此项目

经验公式（希尔记法）:
C16H24N2O3 · HCl
化学文摘社编号:
51781-21-6
分子量:
328.83
MDL number:
MFCD00941499
UNSPSC Code:
41116107
NACRES:
NA.24
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grade

pharmaceutical primary standard

API family

carteolol

form

crystalline powder

shelf life

limited shelf life, expiry date on the label

manufacturer/tradename

BP

application(s)

pharmaceutical
pharmaceutical small molecule

format

neat

storage temp.

2-8°C

SMILES string

[Cl-].[N+H2](C(C)(C)C)CC(O)COc1c2c(ccc1)NC(=O)CC2

InChI

1S/C16H24N2O3.ClH/c1-16(2,3)17-9-11(19)10-21-14-6-4-5-13-12(14)7-8-15(20)18-13;/h4-6,11,17,19H,7-10H2,1-3H3,(H,18,20);1H

InChI key

FYBXRCFPOTXTJF-UHFFFAOYSA-N

General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Carteolol hydrochloride BP Reference standard, intended for use in laboratory tests only as specifically prescribed in the British Pharmacopoeia.

Also used in monographs such as:
  • Carteolol Eye Drops

    • Packaging

    Unit quantity: 100 mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity please visit British Pharmacopoeia

    Other Notes

    Sales restrictions may apply.

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    pictograms

    Exclamation mark
    GHS07

    signalword

    Warning

    hcodes

    H302

    Hazard Classifications

    Acute Tox. 4 Oral

    存储类别

    11 - Combustible Solids

    wgk

    WGK 3

    flash_point_f

    Not applicable

    flash_point_c

    Not applicable

    法规信息

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    分析证书(COA)

    Lot/Batch Number

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    Wen Su et al.
    Frontiers in pharmacology, 11, 202-202 (2020-03-27)
    Carteolol is a non-selective β-adrenoceptor antagonist used for the treatment of glaucoma, and its abuse might be cytotoxic to the cornea. However, its cytotoxicity and underlying mechanisms need to be elucidated. Herein, we used an in vivo model of feline