品質水準
アッセイ
≥99.0% (sum of enantiomers, HPLC)
≥99.0%
形状
powder
光学活性
[α]20/D 77.0 to 82.0°, c = 10% in H2O
分子量
194.18 g/mol
mp
187-195 °C
193-196 °C (lit.)
溶解性
H2O: 0.1 g/mL, clear, colorless
アプリケーション
microbiology
SMILES記法
CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O
InChI
1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6+,7+/m1/s1
InChI Key
HOVAGTYPODGVJG-VEIUFWFVSA-N
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詳細
Methyl α-D-mannopyranoside is a compound that belongs to the class of organic compounds known as o-glycosyl compounds. It is used for the differentiation of Listeria species, Listeria monocytogenes, Listeria innocua, and Listeria welshimeri can ferment the sugar, producing acid which can be identified using an appropriate pH indicator. It has been used to synthesize a series of tri- and tetrahydroxylated seven-membered imino sugars in a study that worked towards a stable Noeuromycin (glycosyl cation mimic that strongly inhibits glycosidases) analog with a D-manno configuration. It has also been used in a study to investigate the primary mannose-binding site of Pradimicin A. (antifungal agent)
アプリケーション
Methyl α-D-mannopyranoside can be used to identify different species of Listeria based on their ability to ferment the sugar.
その他情報
アビジンと内因性レクチンとの好ましくない結合が生じます。
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
404.1 °F
引火点(℃)
206.74 °C
個人用保護具 (PPE)
Eyeshields, Gloves, type N95 (US)
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
67770-BULK:
67770-VAR:
67770-25G:
67770-100G:
67770-500G:
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