所有图片(1)
别名:
C16:0, NSC 5030, 十六酸, 棕榈酸
线性分子式:
CH3(CH2)14COOH
CAS号:
分子量:
256.42
Beilstein:
607489
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24
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等级
pharmaceutical primary standard
蒸汽压
10 mmHg ( 210 °C)
API类
palmitic acid
制造商/商品名称
USP
bp
271.5 °C/100 mmHg (lit.)
mp
61-62.5 °C (lit.)
溶解性
water: 0.00005 g/L at 20 °C
密度
0.852 g/mL at 25 °C (lit.)
应用
pharmaceutical (small molecule)
格式
neat
储存温度
2-8°C
SMILES字符串
CCCCCCCCCCCCCCCC(O)=O
InChI
1S/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)
InChI key
IPCSVZSSVZVIGE-UHFFFAOYSA-N
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一般描述
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.
应用
Palmitic acid USP reference standard for use in specified quality tests and assays.
Also used to prepare standard, and system suitability solutions for assay, and identification tests according to given below monographs of the United States Pharmacopeia (USP):
Also used to prepare standard, and system suitability solutions for assay, and identification tests according to given below monographs of the United States Pharmacopeia (USP):
- Palmitic Acid
- Magnesium Stearate
- Sodium Stearate
- Cetyl Esters Wax
分析说明
These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.
其他说明
Sales restrictions may apply.
WGK
nwg
闪点(°F)
235.4 °F
闪点(°C)
113 °C
Sodium Stearate
United States Pharmacopeia, 39(3), 6024-6024 (2014)
Magnesium Stearate
United States Pharmacopeia, 30(1), 5864-5864 (2016)
Palmitic Acid
United States Pharmacopeia, 42(3), 5918-5918 (2019)
Cetyl Esters Wax
United States Pharmacopeia, 42(5), 5706-5706 (2018)
Andrea Felser et al.
Toxicology, 323, 1-9 (2014-06-03)
Dronedarone is an amiodarone-like antiarrhythmic drug associated with severe liver injury. Since dronedarone inhibits mitochondrial respiration and β-oxidation in vitro, mitochondrial toxicity may also explain dronedarone-associated hepatotoxicity in vivo. We therefore studied hepatotoxicity of dronedarone (200mg/kg/day for 2 weeks or
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