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|---|---|---|---|---|---|---|---|---|---|
| 5g | ¥ ƝȀýôô | > 10 | 4 | -- | > 10 | ¥ NJȀýôô | - + | ||
| 10g | ¥ ƝŲýôô | > 10 | 5 | 6 | 9 | ¥ Ɲôýôô | - + | ||
| 25g | ¥ ŲȀýôô | 4 | 6 | 5 | 6 | ¥ Ȁôýôô | - + | ||
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| 500g | ¥ ǕǕNJƗýôô | > 10 | > 10 | > 10 | 8 | ¥ Ĉƿôýôô | - + | ||
| 1kg | ¥ NJƗôĈýôô | > 10 | 7 | > 10 | > 10 | ¥ ǕƗţƝýôô | - + | ||
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产品编号
1037930
CAS 号
619-05-6
中文名称
3,4-二氨基苯甲酸
MDL 号
MFCD00007726
分子量
152.15
存储条件
2-8°C
网页展示纯度为入库指导纯度值,各批次间存在一定差异,实际纯度以收货为准
熔点
215-218°C
沸点
411.8°C at 760 mmHg
闪点
旋光
描述
TPSA
89.34
LogP
0.5492
H_Acceptors
3
H_Donors
3
Rotatable_Bonds
1
[1]. L A Cooper, et al. Differentiation and melanin production in hyaline and pigmented strains of Microdochium bolleyi. Antonie Van Leeuwenhoek. 1984;50(1):53-62.
[2]. N Sundaraganesan, et al. Vibrational spectra and quantum chemical calculations of 3,4-diaminobenzoic acid. Spectrochim Acta A Mol Biomol Spectrosc. 2008 Jul;70(2):376-83.
[3]. Osmar Calderon Sanchez, et al. (99m)Tc complexes with activated ester functions; ligands comprising a 3,4-diamino-benzoate backbone. Nucl Med Biol. 2006 Apr;33(3):381-90.
[4]. R M Vickers, et al. Clinical laboratory differentiation of Legionellaceae family members with pigment production and fluorescence on media supplemented with aromatic substrates. J Clin Microbiol. 1984 May;19(5):583-7.
[5]. S Ram, et al. Synthesis and biological activity of certain alkyl 5-(alkoxycarbonyl)-1H-benzimidazole-2-carbamates and related derivatives: a new class of potential antineoplastic and antifilarial agents. J Med Chem. 1992 Feb 7;35(3):539-47.
警示图
警示词
Warning
危险申明
H302-H315-H319-H335
警告申明
P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
GHS 编码
GHS07
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售后无忧
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品质保障
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