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2-氨基乙醇硫酸氢酯 | 926-39-6

2-氨基乙醇硫酸氢酯
2-Aminoethyl hydrogen sulfate
926-39-6
C2H7NO4S
141.146279573441
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:2-氨基乙醇硫酸氢酯结构式
70223
名称和标识符
MDL MFCD00008179
InChIKey WSYUEVRAMDSJKL-UHFFFAOYSA-N
Inchi 1S/C2H7NO4S/c3-1-2-7-8(4,5)6/h1-3H2,(H,4,5,6)
SMILES O=S(OCCN)(O)=O
别名信息
- 中文别名 -
  • 2-氨基乙醇硫酸氢酯
  • 2-Aminoethyl Hydrogen Sulfate 2-氨基乙醇硫酸氢酯
  • 2-氨基乙基硫化氢
  • 2-氨基乙基硫氢酸
  • 2-氨基乙基硫酸氢钠
  • 2-氨基乙基硫酸氢酯
  • 2-氨乙基硫酸酯
  • 硫酸氢二氨基乙酯
  • 氨乙醇硫酸氢酯
- 英文别名 -
  • 2-Aminoethyl hydrogen sulfate
  • Sulfuric Acid Mono(2-Aminoethyl) Ester
  • 2-Aminoethyl hyorogen sulfate
  • 2-AMINOETHYL SULFATE
  • Ethanol, 2-amino-,1-(hydrogen sulfate)
  • Ethanol, 2-amino-, hydrogen sulfate (7CI)
  • Ethanol, 2-amino-, hydrogen sulfate (ester) (8CI, 9CI)
  • Ethanol, 2-amino-, sulfate (6CI)
  • (2-Aminoethoxy)sulfonic acid
  • 2-Aminoethanol hydrogen sulfate (ester)
  • 2-Aminoethyl sulfate
  • 2-Aminoethyl sulfuric acid
  • 2-Azaniumylethyl sulfate
  • Ethanolamine O-sulfate
  • Ethanolamine sulfate
  • Mono(2-aminoethyl) sulfate
  • NSC 204188
  • NSC 3532
  • WAS-34
  • Sulfuric Acid Mono(2-aminoethyl) Ester
物化性质
实验特性
LogP 0.54560
PSA 98.00000
折射率 1.5130 (estimate)
水溶性 almost transparency
熔点 279°C(dec.)(lit.)
颜色与性状 白色结晶性粉末。无腐蚀性。
溶解性 溶于水,不溶于多数有机溶剂。
密度 1.344 (estimate)
计算特性
精确分子量 141.01000
氢键供体数量 2
氢键受体数量 5
可旋转化学键数量 3
重原子数量 8
复杂度 133
同位素原子数量 0
确定原子立构中心数量 0
不确定原子立构中心数量 0
确定化学键立构中心数量 0
不确定化学键立构中心数量 0
共价键单元数量 1
疏水参数计算参考值(XlogP) -4.1
互变异构体数量
表面电荷 0
国际标准相关数据
EINECS 213-135-7
海关数据
海关编码 2922199090
海关数据

中国海关编码:

2922199090

概述:

2922199090. 其他氨基醇及其醚,酯和它们的盐(但含一种以上含氧基的除外). 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, 乙醇胺及其盐应报明色度, 乙醇胺及其盐应报明包装

Summary:

2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

合成路线

合成路线:1 步

反应条件:
参考文献:
Synthesis of taurine
Bondareva, O. M.; Lopatik, D. V.; Kuvaeva, Z. I.; Vinokurova, L. G.; Markovich, M. M.; et al, Pharmaceutical Chemistry Journal, 2008, 42(3), 142-144

合成路线:1 步

反应条件:
参考文献:
Process for the preparation of cysteamine bitartrate and product so obtained
, United States, , ,

合成路线:1 步

反应条件:
参考文献:
Improved technology for synthesis of taurine
Yang, Jie; Liu, Yongqiong; Zhu, Hong; Bai, Zhengwu; Zou, Ying, Huagong Jinzhan, 2005, 24(11), 1269-1272

合成路线:1 步

反应条件:
参考文献:
Process for preparation of cysteamine hydrochloride via basic hydrolysis
, China, , ,

合成路线:1 步

反应条件:
参考文献:
Synthesis and biological activity of novel 2-thiazolidinone sulfonylurea derivatives
Chen, Qing-wu; Shen, De-long, Zhejiang Gongye Daxue Xuebao, 2008, 36(5), 562-564

合成路线:1 步

反应条件:
参考文献:
Method for preparing granular ethanolamine sulfate ester crystal by adding habit modifier and seed crystal slurry
, China, , ,

合成路线:1 步

反应条件:
参考文献:
Preparation method of branched polyethyleneimine and shale intercalation inhibitor
, China, , ,

合成路线:1 步

反应条件:
参考文献:
Synthetic method and application of 3-benzyl-1,3-thiazole-2-thioketone
, China, , ,

合成路线:1 步

反应条件:
参考文献:
Circulating method for producing taurine from ethanolamine
, China, , ,

合成路线:1 步

反应条件:
参考文献:
Synthesis and biological evaluation of thiazolidine-2-thione derivatives as novel xanthine oxidase inhibitors
Wang, Mu-Xuan; Qin, Hong-Wei; Liu, Chao ; Lv, Shen-Ming; Chen, Jia-Shu; et al, PLoS One, 2022, 17(5),

合成路线:1 步

反应条件:
参考文献:
Process for the preparation of aziridine crosslinking agent
, China, , ,

合成路线:1 步

反应条件:
参考文献:
(2-Aminoethyl)sulfuric acid betaine from hydroxyethylcarbamic acid betaine
Pascoe, Peter F., Justus Liebigs Annalen der Chemie, 1967, 708, 69-71

合成路线:1 步

反应条件:
参考文献:
Synthesis and physicochemical and antimicrobial properties of 2-(2-hydroxyalkylamino)ethanesulfonic acids
Kanetani, Fujio; Tanaka, Tadashi; Nakano, Shinji; Negoro, Kenji, Nippon Kagaku Kaishi, 1982, (5), 824-9

合成路线:1 步

反应条件:
参考文献:
Method for synthesizing 2-aminoethanol sulfate as precursor of taurine
, China, , ,

合成路线:1 步

反应条件:
参考文献:
Process for preparing sulfuric acid monoesters of aminoalkanols
, World Intellectual Property Organization, , ,

合成路线:1 步

反应条件:
参考文献:
Synthesis of taurine by esterification of ethanolamine
Tang, Hong-ke; Chen, Jun-zhi; Ma, Yu; Zou, Xiang-long, Shiyou Huagong, 2002, 31(4), 279-282

合成路线:1 步

反应条件:
参考文献:
Modification of Wenker's method of preparing ethylenimine
Leighton, Philip A.; Perkins, Wm. A.; Renquist, Melvin L., Journal of the American Chemical Society, 1947, 69,

合成路线:1 步

反应条件:
参考文献:
Design and synthesis of 3-(1-phenylethyl)thiazolidine-2-thione derivatives with potential biological activities
Li, Hong-xin; Chen, Xiao-tao; Xu, Liang-zhong, Chemical Research in Chinese Universities, 2011, 27(3), 431-434

合成路线:1 步

反应条件:
参考文献:
Formation and transformation of esters. LVI. Effect of sulfuric acid on amino alcohols
Cherbuliez, Emile; Chapalay, C.; Colak-Antic, Sl.; Marszalek, J.; Vallet, L.; et al, Helvetica Chimica Acta, 1964, 47(7), 2106-12

合成路线:1 步

反应条件:
参考文献:
Process for making biobased products from sugars
, World Intellectual Property Organization, , ,
相关文献
  • 1. 593. Acid dissociation constants of the ammonium group in 2-aminoethanol, 2-aminoethyl phosphate, and 2-aminoethyl sulphate
    S. P. Datta,A. K. Grzybowski J. Chem. Soc. 1962 3068
  • 2. Amino-alkanethiols from amino-alcohols via aminoalkyl sulphates and thiazolidinethiones
    Terence C. Owen J. Chem. Soc. C 1967 1373
  • 3. Amino-alkanethiols from amino-alcohols via aminoalkyl sulphates and thiazolidinethiones
    Terence C. Owen J. Chem. Soc. C 1967 1373
  • 4. 474. The ionization of ethyleneimine and polyethyleneimine
    E. J. Shepherd,J. A. Kitchener J. Chem. Soc. 1956 2448
  • 5. Adsorption and separation of cations on silica gel chemically modified by homogeneous and heterogeneous routes with the ethylenimine anchored on thiol modified silica gel
    Alexandre G. S. Prado,Luiza N. H. Arakaki,Claudio Airoldi Green Chem. 2002 4 42
  • 6. Kinetics of formation of substituted styrene oxides by reaction of 2-aryl- and 1-aryl-2-halogenoethanols with aqueous alkali
    Anthony C. Knipe J. Chem. Soc. Perkin Trans. 2 1973 589
  • 7. Chapter 14. Biological chemistry. Part (iv) Enzyme chemistry
    M. C. Summers,D. C. Williams Annu. Rep. Prog. Chem. Sect. B: Org. Chem. 1977 74 432
  • 8. 222. The stability constants of the silver complexes of some aliphatic amines and amino-acids
    S. P. Datta,A. K. Grzybowski J. Chem. Soc. 1959 1091
  • 9. 565. Hydrogen bonding in gaseous mixtures. Part V. Infrared spectra of amine–alcohol systems
    D. J. Millen,J. Zabicky J. Chem. Soc. 1965 3080
  • 10. Journal: index of subjects, 1962
    J. Chem. Soc. 1962 5337
专业数据库参考
PubChemId 70223
参考资料
Reaxys RN 1704079
Beilstein 4(4)1414
化合物详情(旧版)

SMILES

NCCOS(=O)(O)=O

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