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Merck
CN

1.12120

SAFC

碳酸钙

precipitated (≤ 0.0001% Al), EMPROVE® ESSENTIAL, Ph. Eur., BP, JP, USP, FCC, E 170

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About This Item

线性分子式:
CaCO3
CAS号:
分子量:
100.09
Beilstein:
8008338
MDL编号:
UNSPSC代码:
12352302
E编号:
E170
EC索引号:
207-439-9

Agency

BP
JP
Ph. Eur.
USP

质量水平

管理合规性

FCC

产品线

EMPROVE® ESSENTIAL

形式

solid

效能

6450 mg/kg LD50, oral (Rat)
>2000 mg/kg LD50, skin (Rat)

pH值(酸碱度)

9.5-10.5 (20 °C, 100 g/L in H2O, slurry)

mp

825 °C (decomposition)

密度

2.93 g/mL at 25 °C (lit.)

应用

liquid formulation
pharmaceutical
solid formulation

储存温度

2-30°C

SMILES字符串

[Ca++].[O-]C([O-])=O

InChI

1S/CH2O3.Ca/c2-1(3)4;/h(H2,2,3,4);/q;+2/p-2

InChI key

VTYYLEPIZMXCLO-UHFFFAOYSA-L

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一般描述

Finding the right excipient that matches your needs as well as regulatory demands can be a complicated challenge in formulation. With our application know-how and regulatory expertise, we support you in every step of development, scale-up, and production.
As part of our Emprove® Program, our raw materials are offered with extensive documentation facilitating compliance of your pharma and biopharma product, full supply chain transparency and risk mitigation. Our SAFC® portfolio of high-quality products for biopharmaceutical and pharmaceutical formulation and production withstands strict quality control procedures and is produced according to applicable cGMP guidelines.

应用

Calcium carbonate is typically used as alkalizer or mineral supplement in solid formulations. The low aluminum content is relevant for baby food application.

法律信息

Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany
SAFC is a registered trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

13 - Non Combustible Solids

WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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J P Hilton-Proctor et al.
European journal of medicinal chemistry, 191, 112120-112120 (2020-03-03)
N-Methylpyrrolidone is one of several chemotypes that have been described as a mimetic of acetyl-lysine in the development of bromodomain inhibitors. In this paper, we describe the synthesis of a 4-phenyl substituted analogue - 1-methyl-4-phenylpyrrolidin-2-one - and the use of

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