推荐产品
化驗
95%
形狀
solid
SMILES 字串
Nc1ccccc1S(O)(=O)=O
InChI
1S/C6H7NO3S/c7-5-3-1-2-4-6(5)11(8,9)10/h1-4H,7H2,(H,8,9,10)
InChI 密鑰
ZMCHBSMFKQYNKA-UHFFFAOYSA-N
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訊號詞
Danger
危險聲明
危險分類
Skin Corr. 1B
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
其他客户在看
Po-Hsin Wang et al.
Nanomaterials (Basel, Switzerland), 8(4) (2018-04-05)
In this work, we electrochemically deposited self-doped polyanilines (SPANI) on the surface of carbon-nanoparticle (CNP) film, enhancing the superficial faradic reactions in supercapacitors and thus improving their performance. SPANI was electrodeposited on the CNP-film employing electropolymerization of aniline (AN) and
T Thurnheer et al.
Biodegradation, 1(1), 55-64 (1990-01-01)
Alcaligenes sp. strain O-1 grew with benzene sulfonate (BS) as sole carbon source for growth with either NH4+ or NH4+ plus orthanilate (2-aminobenzene sulfonate, OS) as the source(s) of nitrogen. The intracellular desulfonative enzyme did not degrade 3- or 4-aminobenzene
J Mampel et al.
Microbiology (Reading, England), 145 ( Pt 11), 3255-3264 (1999-12-10)
Growth of Alcaligenes sp. strain O-1 with 2-aminobenzenesulfonate (ABS; orthanilate) as sole source of carbon and energy requires expression of the soluble, multicomponent 2-aminobenzenesulfonate 2,3-dioxygenase system (deaminating) (ABSDOS) which is plasmid-encoded. ABSDOS was separated by anion-exchange chromatography to yield a
Inotropic activity of orthanilic and L-cysteic acid on isolated guinea-pig ventricular strips.
F Franconi et al.
Advances in experimental medicine and biology, 217, 159-165 (1987-01-01)
F Junker et al.
The Biochemical journal, 300 ( Pt 2), 429-436 (1994-06-01)
2-Aminobenzenesulphonic acid (2AS) is degraded by Alcaligenes sp. strain O-1 via a previously detected but unidentified intermediate. A mutant of strain O-1 was found to excrete this intermediate, which was isolated and identified by m.s., 1H- and 13C-n.m.r. as 3-sulphocatechol
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