所有图片(1)
About This Item
经验公式（希尔记法）:
C27D6H38O2 · H2O
CAS号:
分子量:
424.69
UNSPSC代码:
12352106
PubChem化学物质编号:
NACRES:
NA.12
同位素纯度
98 atom % D
质量水平
检测方案
97% (CP)
形式
powder
技术
mass spectrometry (MS): suitable
颜色
white to off-white
应用
detection
质量偏移
M+6
储存温度
−20°C
SMILES字符串
C[C@]1(CCC/2)C(CCC1[C@H](C)CCCC(O)(C([2H])([2H])[2H])C([2H])([2H])[2H])C2=C\C=C(C[C@@H](O)CC3)/C3=C.[H]O[H]
InChI
1S/C27H44O2.H2O/c1-19-10-13-23(28)18-22(19)12-11-21-9-7-17-27(5)24(14-15-25(21)27)20(2)8-6-16-26(3,4)29;/h11-12,20,23-25,28-29H,1,6-10,13-18H2,2-5H3;1H2/b21-11+,22-12-;/t20-,23+,24?,25?,27-;/m1./s1/i3D3,4D3;
InChI key
WRLFSJXJGJBFJQ-DZAJWRDGSA-N
一般描述
25-hydroxyvitamin D3 (calcifediol) is a prohormone produced via hydroxylation of vitamin D3 (cholecalciferol) in the liver. It is a precursor for the synthesis of calcitriol {1,25-dihydroxyvitamin D3 or [1,25(OH)2D3]}. It is used as a biomarker to determine the status of vitamin D in the body.
25-Hydroxyvitamin D3-26,26,26,27,27,27-d6 monohydrate is a deuterated vitamin D3 wherein methyl protons of C-26, C-27 carbons are replaced by deuterium.
25-Hydroxyvitamin D3-26,26,26,27,27,27-d6 monohydrate is a deuterated vitamin D3 wherein methyl protons of C-26, C-27 carbons are replaced by deuterium.
应用
25-Hydroxyvitamin D3-26,26,26,27,27,27-d6 monohydrate can be used as a stable isotope internal standard for data interpretation in specific biological samples by mass spectrometry.
包装
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
警示用语：
Danger
危险分类
Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - STOT RE 1 Oral
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
美国出口管控1C298产品
25-Hydroxyvitamin D3, the prohormone of 1, 25-dihydroxyvitamin D3, inhibits the proliferation of primary prostatic epithelial cells
Barreto, AM et al.
Cancer Epidemiology, Biomarkers & Prevention, 9(3), 265-270 (2000)
Quantification of circulating 25-hydroxyvitamin D by liquid chromatography-tandem mass spectrometry
Vogeser M
The Journal of Steroid Biochemistry and Molecular Biology, 121(3-5), 565-573 (2010)
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