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等級
technical grade
折射率
n20/D 1.530 (lit.)
bp
170 °C (lit.)
溶解度
alcohol: freely soluble
chloroform: freely soluble
diethyl ether: freely soluble
密度
1.117 g/mL at 25 °C (lit.)
官能基
hydroxyl
nitrile
phenyl
SMILES 字串
OC(C#N)c1ccccc1
InChI
1S/C8H7NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8,10H
InChI 密鑰
NNICRUQPODTGRU-UHFFFAOYSA-N
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應用
Mandelonitrile has been used to extract mandeloamide by the nitrilase variants[1].
訊號詞
Danger
危險分類
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1
儲存類別代碼
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
水污染物質分類（WGK）
WGK 3
閃點（°F）
206.6 °F - closed cup
閃點（°C）
97 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Zhi-Jun Zhang et al.
Bioprocess and biosystems engineering, 34(3), 315-322 (2010-10-21)
A nitrilase gene from Alcaligenes sp. ECU0401 was cloned and overexpressed in Escherichia coli BL21 (DE3) in a soluble form. The encoded protein with a His₆-tag was purified to nearly homogeneity as revealed by SDS-PAGE with a molecular weight of
Aem Nuylert et al.
Chembiochem : a European journal of chemical biology, 18(3), 257-265 (2016-12-04)
A hydroxynitrile lyase from the passion fruit Passiflora edulis (PeHNL) was isolated from the leaves and showed high stability in biphasic co-organic solvent systems for cyanohydrin synthesis. Cyanohydrins are important building blocks for the production of fine chemicals and pharmaceuticals.
Hualei Wang et al.
BMC biotechnology, 13, 14-14 (2013-02-19)
A nitrilase-mediated pathway has significant advantages in the production of optically pure (R)-(-)-mandelic acid. However, unwanted byproduct, low enantioselectivity, and specific activity reduce its value in practical applications. An ideal nitrilase that can efficiently hydrolyze mandelonitrile to optically pure (R)-(-)-mandelic
Jennifer L Seffernick et al.
Journal of biotechnology, 143(1), 17-26 (2009-06-23)
Mining sequence data is increasingly important for biocatalysis research. However, when relying on sequence data alone, prediction of the reaction catalyzed by a specific protein sequence is often elusive, and substrate specificity is far from trivial. The present study demonstrated
Nisha Jangir et al.
Bioorganic chemistry, 84, 32-40 (2018-11-28)
Hydroxynitrile lyase (HNL) catalyzed enantioselective CC bond formation is an efficient approach to synthesize chiral cyanohydrins which are important building blocks in the synthesis of a number of fine chemicals, agrochemicals and pharmaceuticals. Immobilization of HNL is known to provide
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