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Merck
CN

51230

Sigma-Aldrich

Hematein

suitable for microscopy

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关于此项目

经验公式(希尔记法):
C16H12O6
CAS Number:
分子量:
300.26
颜色索引号:
75290
Beilstein:
93039
EC 号:
MDL编号:
UNSPSC代码:
12171500
PubChem化学物质编号:
NACRES:
NA.47
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表单

powder

质量水平

浓度

≥40% (UV)

mp

140 °C

λmax

425-435 nm

适用性

suitable for microscopy

应用

diagnostic assay manufacturing
hematology
histology

储存温度

room temp

SMILES字符串

Oc1ccc2c(OCC3(O)CC4=CC(=O)C(O)=CC4=C23)c1O

InChI

1S/C16H12O6/c17-10-2-1-8-13-9-4-12(19)11(18)3-7(9)5-16(13,21)6-22-15(8)14(10)20/h1-4,17,19-21H,5-6H2

InChI key

HLUCICHZHWJHLL-UHFFFAOYSA-N

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储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Effect of formalin pigment removal on peroxidase-antiperoxidase immunoperoxidase technique.
J McGovern et al.
Journal of clinical pathology, 39(8), 923-925 (1986-08-01)
G T Oh et al.
Atherosclerosis, 159(1), 17-26 (2001-11-02)
Hematein is a compound isolated from Caesalpinia sappan that has been used in oriental medicine as both an analgesic and an anti-inflammatory agent. In this study, we examined the anti-atherogenic potential of hematein using cholesterol-fed New Zealand White (NZW) rabbits.
Alison N Hulme et al.
Phytochemistry, 66(23), 2766-2770 (2005-10-26)
The electrospray ionisation mass spectra of the neoflavanoids brazilin and hematoxylin are reported in both their reduced (1 and 2, respectively) and their oxidised forms (3 and 4, respectively). In the reduced forms, breakdown pathways under collision induced decomposition (CID)
M T Panayotacopoulou et al.
Journal of neurocytology, 18(5), 593-597 (1989-10-01)
Protein bodies in catecholamine neurons of the normal human brain contain arginine-rich proteins similar to those present in the core of Lewy bodies in Parkinsonian brains. Lewy bodies are known also to contain phospholipids in their core, demonstrable with Baker's
C Bettinger et al.
Histochemistry, 95(3), 279-288 (1991-01-01)
Analytically pure hematoxylin (Htx), pentaacetylhematoxylin (PAHtx), and hematein (Hm) were isolated and characterized by 1H-NMR spectroscopy. The VIS/UV spectra of Htx and Hm were recorded in MeOH and in H2O at various pH values. The molar extinction coefficients of the

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