| 规格 | 目录价格 | 上海 | 安徽 | 武汉 | 成都 | 北方 | 深圳 | 会员价格 | 数量 |
|---|---|---|---|---|---|---|---|---|---|
| 5g | ¥ ǦľĝŠŠ | -- | -- | -- | -- | -- | -- | ¥ ǦľĝŠŠ | - + |
| 5g | ¥ ȫŹĝŠŠ | -- | -- | -- | 1 | -- | 1 | ¥ ȫŹĝŠŠ | - + |
| 1g | ¥ ƣŕŠĝŠŠ | -- | -- | -- | -- | -- | -- | ¥ ƣŕŠĝŠŠ | - + |
| 5g | ¥ ȫǦȫĝŠŠ | -- | -- | -- | -- | -- | -- | ¥ ȫǦȫĝŠŠ | - + |
| 5g | ¥ ྏĝŠŠ | -- | -- | 1 | 4 | -- | 1 | ¥ ྏĝŠŠ | - + |
| 1kg | ¥ ƣľŠľĝŠŠ | -- | -- | -- | ¥ ƣľŠľĝŠŠ | - + | |||
| 大货 | 请询价 | -- | -- | -- | -- | -- | -- | -- | - + |
[1]. Mitchell SC, et al. Fate of thianthrene in biological systems. Xenobiotica. 17 Aug;47(8):731-74.
[]. Alfonso Pérez-Garrido, et al. Convenient QSAR model for predicting the complexation of structurally diverse compounds with beta-cyclodextrins. Bioorg Med Chem. 9 Jan 15;17():896-94.
[3]. C SEROWY, et al. [Experiences with thianthrol salve in dermatology]. Z Haut Geschlechtskr. 1951 May 1;1(9):37-6.
[4]. D A SHIRLEY, et al. Formation of thianthrene by a free radical mechanism. Science. 1951 Feb 3;113(93):8-1.
[5]. Daniele Casarini, et al. Ring inversion dynamics of derivatives of thianthrene di- and tetraoxide. J Org Chem. 6 Aug 4;71(16):648-5.
H3-H315-H319-H335
P61-P64-P7-P71-P8-P3+P35-P34+P34-P35+P351+P338-P33-P36+P364-P43+P33-P45-P51
GHS7
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