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甘氨酰胺盐酸盐

甘氨酰胺盐酸盐用途

2-氨基乙酰胺盐酸盐是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。

甘氨酰胺盐酸盐名称

[ CAS 号 ]:
1668-10-6

[ 中文名 ]:
甘氨酰胺盐酸盐

[ 英文名 ]:
H-Gly-NH2.HCl

[中文别名 ]:

[英文别名 ]:

Acetamide, 2-amino-, monohydrochloride
2-Aminoacetamide hydrochloride
Glycinamide hydrochloride (1:1)
MFCD00013008
Glycine amide hydrochloride
Glycinamide, monohydrochloride
EINECS 216-789-1
2-aminoacetamide,hydrochloride
Acetamide, 2-amino-, hydrochloride (1:1)
H-Gly-NH2.HCl

甘氨酰胺盐酸盐生物活性

[ 描述 ]:

2-氨基乙酰胺盐酸盐是一种生物化学试剂,可作为生物材料或有机化合物用于生命科学相关研究。

[ 相关类别 ]:

研究领域 >> 其他

信号通路 >> 其他 >> 其他

甘氨酰胺盐酸盐物理化学性质

[ 密度 ]:
1.122g/cm3

[ 沸点 ]:
281.3ºC at 760mmHg

[ 熔点 ]:
204 °C (dec.)(lit.)

[ 分子式 ]:
C₂H₇ClN₂O

[ 分子量 ]:
110.54

[ 精确质量 ]:
110.024689

[ PSA ]:
69.11000

[ LogP ]:
0.63300

[ 外观性状 ]:
白色至灰白色固体

[ 蒸汽压 ]:
0.00359mmHg at 25°C

[ 储存条件 ]:
Store at RT.

[ 水溶解性 ]:
H2O: 0.1 g/mL, clear

甘氨酰胺盐酸盐MSDS

详细MSDS(安全技术说明书)

甘氨酰胺盐酸盐安全信息

[ 个人防护装备 ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ 危害码 (欧洲) ]:
Xi:Irritant

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S22-S24/25-S37/39-S26

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

[ 海关编码 ]:
29241900

甘氨酰胺盐酸盐上下游产品

甘氨酰胺盐酸盐上游产品

甘氨酰胺盐酸盐下游产品

甘氨酰胺盐酸盐制备

由氯乙酸甲酯经胺化而得。将氨水冷却至0℃以下，滴加氯乙酸甲酯，保温2h。于20℃以下通氨至预定量，静置反应8h后，排除余氨，升温至60℃，减压浓缩，得氨基乙酰胺盐酸盐。

甘氨酰胺盐酸盐海关

[ 海关编码 ]: 2924199090

[ 中文概述 ]:
2924199090. 其他无环酰胺（包括无环氨基甲酸酯)(包括其衍生物及盐）. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 包装

[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

甘氨酰胺盐酸盐文献

Preparation of guanine and diaminopurine from biuret. Part III.

Chem. Biodivers. 4(4) , 818-22, (2007)

Because of their potential prebiotic origin and relative chemical stability, urea, biuret, formic acid, and glycine amide might have played a role in the assembly process of purine bases. In this pape...

Identification of quinoline, carboline and glycinamide compounds in cow milk using HRMS and NMR.

Food Chem. 141(3) , 1888-94, (2013)

The aim of this work was to characterise new UV-absorbing compounds (UAC) in cow milk in order to gain an overview of the molecular diversity of the minor bioactive constituents, that could be used to...

Synthesis of (-)-quinocarcin by directed condensation of alpha-amino aldehydes.

J. Am. Chem. Soc. 127(48) , 16796-7, (2005)

An enantioselective synthesis of the natural antiproliferative agent quinocarcin was achieved by the directed condensation of optically active alpha-amino aldehyde intermediates. Condensation of the N...

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