Bismuth subcarbonate structure
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Common Name | Bismuth subcarbonate | ||
|---|---|---|---|---|
| CAS Number | 5892-10-4 | Molecular Weight | 509.969 | |
| Density | 6.86 g/mL at 25 °C(lit.) | Boiling Point | 333.6ºC at 760mmHg | |
| Molecular Formula | CBi2O5 | Melting Point | 308(分解)ºC | |
| MSDS | Chinese USA | Flash Point | 169.8ºC | |
Use of Bismuth subcarbonateBismuth subcarbonate (Bismuth carbonate oxide) is a typical Bi-based semiconductor that is widely applied as antibacterial, sensors, super capacitors, and photocatalysts. Bismuth subcarbonate protects the gastric ulcer from further erosion by gastric acid[1][2]. |
| Name | Bismuth subcarbonate |
|---|---|
| Synonym | More Synonyms |
| Description | Bismuth subcarbonate (Bismuth carbonate oxide) is a typical Bi-based semiconductor that is widely applied as antibacterial, sensors, super capacitors, and photocatalysts. Bismuth subcarbonate protects the gastric ulcer from further erosion by gastric acid[1][2]. |
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| Related Catalog | |
| References |
[2]. Rimsha Ali, et al. Milk-Alkali Syndrome. StatPearls [Internet]. 2021 Jan. |
| Density | 6.86 g/mL at 25 °C(lit.) |
|---|---|
| Boiling Point | 333.6ºC at 760mmHg |
| Melting Point | 308(分解)ºC |
| Molecular Formula | CBi2O5 |
| Molecular Weight | 509.969 |
| Flash Point | 169.8ºC |
| Exact Mass | 509.935364 |
| PSA | 69.67000 |
| InChIKey | MGLUJXPJRXTKJM-UHFFFAOYSA-L |
| SMILES | O=[Bi]OC(=O)O[Bi]=O |
| Stability | Stable. |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| Safety Phrases | S22-S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2836999000 |
| HS Code | 2836999000 |
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[Experimental studies on altering the properties of the prosthetic plastic, Kallocryl B, by adding an x-ray contrast medium].
Stomatol. DDR 30(7) , 475-81, (1980)
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[In vitro studies on effect of particle size of bismuth subcarbonate on antacid effectiveness].
Yao Xue Xue Bao 18(8) , 630-2, (1983)
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Bismuth subgallate/borneol (suile) is superior to bacitracin in the human forearm biopsy model for acute wound healing.
Adv. Skin Wound Care 20(9 Pt 1) , 485-92, (2007) The human forearm biopsy model can evaluate the effect of novel agents on acute wounds. Bismuth subgallate/borneol (Suile) is a new product cleared by the Food and Drug Administration for treating par... |
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Name: qHTS assay to identify small molecule antagonists of the androgen receptor (AR) signa...
Source: 824
Target: AR protein [Homo sapiens]
External Id: MDAN535
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Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
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Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
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Name: qHTS assay to identify small molecule antagonists of the androgen receptor (AR) sign...
Source: 824
Target: N/A
External Id: MDAV150
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Name: qHTS assay for small molecules that induce genotoxicity in human embryonic kidney cel...
Source: 824
Target: RecName: Full=ATPase family AAA domain-containing protein 5; AltName: Full=Chromosome fragility-associated gene 1 protein
External Id: ELG271
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Name: qHTS assay to identify small molecule antagonists of the thyroid receptor (TR) signal...
Source: 824
Target: thyroid hormone receptor beta isoform 2 [Rattus norvegicus]
External Id: TRN186
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Name: qHTS assay to identify small molecule antagonists of the thyroid receptor (TR) signal...
Source: 824
Target: N/A
External Id: TRV455
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Name: S16 Schwann cell viability assay (CellTiter-Glo assay)
Source: NCGC
Target: N/A
External Id: cmt-p4-fda-celltiter_regid
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Name: Biochemical firefly luciferase enzyme assay for NPC
Source: NCGC
Target: Luciferase [Photinus pyralis]
External Id: adst-fluc-km-fda-o1_regid
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Name: Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screeni...
Source: NCGC
Target: N/A
External Id: CPF001
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| MFCD00010877 |
| EINECS 227-567-9 |
| 1,3,5-Trioxo-2,4-dioxa-1,5-dibismapentane |
| Bismuth(III) carbonate basic |
| bis(oxobismuthanyl) carbonate |