- Method for synthesizing 2-aminoethanol sulfate as precursor of taurine, China, , ,
Cas no 926-39-6 (2-Aminoethyl hydrogen sulfate)
2-Aminoethyl hydrogen sulfate Chemical and Physical Properties
Names and Identifiers
-
- 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 sulfuric acid
- 2-Azaniumylethyl sulfate
- Ethanolamine O-sulfate
- Ethanolamine sulfate
- Mono(2-aminoethyl) sulfate
- NSC 204188
- NSC 3532
- WAS-34
-
- MDL: MFCD00008179
- Inchi: 1S/C2H7NO4S/c3-1-2-7-8(4,5)6/h1-3H2,(H,4,5,6)
- InChI Key: WSYUEVRAMDSJKL-UHFFFAOYSA-N
- SMILES: O=S(OCCN)(O)=O
Computed Properties
- Exact Mass: 141.01000
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 8
- Rotatable Bond Count: 3
- Complexity: 133
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: -4.1
Experimental Properties
- Color/Form: White crystalline powder. Non corrosive.
- Density: 1.344 (estimate)
- Melting Point: 279°C(dec.)(lit.)
- Refractive Index: 1.5130 (estimate)
- Water Partition Coefficient: almost transparency
- PSA: 98.00000
- LogP: 0.54560
- Solubility: Soluble in water, insoluble in most organic solvents.
2-Aminoethyl hydrogen sulfate Security Information
-
Symbol:
- Prompt:warning
- Signal Word:Warning
- Hazard Statement: H302-H315-H319
- Warning Statement: P264-P270-P280-P301+P312+P330-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P501
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:3
- Hazard Category Code: 22-36/37/38
- Safety Instruction: S26-S36
- RTECS:KJ6371000
-
Hazardous Material Identification:
- Risk Phrases:R22
- Storage Condition:Sealed in dry,Room Temperature
2-Aminoethyl hydrogen sulfate Customs Data
- HS CODE:2922199090
- Customs Data:
China Customs Code:
2922199090Overview:
2922199090. Other amino alcohols and their ethers,Esters and their salts(Except those containing more than one oxygen-containing group). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to, The color of ethanolamine and its salt should be reported, The package of ethanolamine and its salt shall be declared
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%
2-Aminoethyl hydrogen sulfate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | A609545-50g |
2-Aminoethyl Sulfate |
926-39-6 | 50g |
$ 173.00 | 2023-09-08 | ||
| TRC | A609545-100g |
2-Aminoethyl Sulfate |
926-39-6 | 100g |
$ 201.00 | 2023-09-08 | ||
| TRC | A609545-250g |
2-Aminoethyl Sulfate |
926-39-6 | 250g |
$ 443.00 | 2023-09-08 | ||
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A151387-25g |
2-Aminoethyl hydrogen sulfate |
926-39-6 | >98.0%(T) | 25g |
¥79.90 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A151387-5g |
2-Aminoethyl hydrogen sulfate |
926-39-6 | >98.0%(T) | 5g |
¥33.90 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A151387-500g |
2-Aminoethyl hydrogen sulfate |
926-39-6 | >98.0%(T) | 500g |
¥987.90 | 2023-09-04 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | A151387-100g |
2-Aminoethyl hydrogen sulfate |
926-39-6 | >98.0%(T) | 100g |
¥288.90 | 2023-09-04 | |
| Fluorochem | 226245-1g |
2-Aminoethyl hydrogen sulfate |
926-39-6 | 97% | 1g |
£10.00 | 2022-02-28 | |
| Fluorochem | 226245-25g |
2-Aminoethyl hydrogen sulfate |
926-39-6 | 97% | 25g |
£14.00 | 2022-02-28 | |
| Fluorochem | 226245-100g |
2-Aminoethyl hydrogen sulfate |
926-39-6 | 97% | 100g |
£40.00 | 2022-02-28 |
2-Aminoethyl hydrogen sulfate Production Method
Production Method 1
Production Method 2
- Method for preparing granular ethanolamine sulfate ester crystal by adding habit modifier and seed crystal slurry, China, , ,
Production Method 3
- Synthesis of taurine by esterification of ethanolamineTang, Hong-ke; Chen, Jun-zhi; Ma, Yu; Zou, Xiang-long, Shiyou Huagong, 2002, 31(4), 279-282
Production Method 4
- Process for the preparation of aziridine crosslinking agent, China, , ,
Production Method 5
- Synthesis and physicochemical and antimicrobial properties of 2-(2-hydroxyalkylamino)ethanesulfonic acidsKanetani, Fujio; Tanaka, Tadashi; Nakano, Shinji; Negoro, Kenji, Nippon Kagaku Kaishi, 1982, (5), 824-9
Production Method 6
- Design and synthesis of 3-(1-phenylethyl)thiazolidine-2-thione derivatives with potential biological activitiesLi, Hong-xin; Chen, Xiao-tao; Xu, Liang-zhong, Chemical Research in Chinese Universities, 2011, 27(3), 431-434
Production Method 7
- Process for making biobased products from sugars, World Intellectual Property Organization, , ,
Production Method 8
- Synthesis of taurineBondareva, O. M.; Lopatik, D. V.; Kuvaeva, Z. I.; Vinokurova, L. G.; Markovich, M. M.; et al, Pharmaceutical Chemistry Journal, 2008, 42(3), 142-144
Production Method 9
- Improved technology for synthesis of taurineYang, Jie; Liu, Yongqiong; Zhu, Hong; Bai, Zhengwu; Zou, Ying, Huagong Jinzhan, 2005, 24(11), 1269-1272
Production Method 10
1.2 Reagents: Sodium hydroxide Solvents: Water ; pH 10.7
- Process for preparing sulfuric acid monoesters of aminoalkanols, World Intellectual Property Organization, , ,
Production Method 11
- Preparation method of branched polyethyleneimine and shale intercalation inhibitor, China, , ,
Production Method 12
- Synthesis and biological evaluation of thiazolidine-2-thione derivatives as novel xanthine oxidase inhibitorsWang, Mu-Xuan; Qin, Hong-Wei; Liu, Chao ; Lv, Shen-Ming; Chen, Jia-Shu; et al, PLoS One, 2022, 17(5),
Production Method 13
Production Method 14
1.2 Reagents: Carbon disulfide , Sodium hydroxide Solvents: Water ; rt; rt → 45 °C; 2 h, 45 °C; 45 °C → 55 °C
- Process for preparation of cysteamine hydrochloride via basic hydrolysis, China, , ,
Production Method 15
- Modification of Wenker's method of preparing ethylenimineLeighton, Philip A.; Perkins, Wm. A.; Renquist, Melvin L., Journal of the American Chemical Society, 1947, 69,
Production Method 16
- Process for the preparation of cysteamine bitartrate and product so obtained, United States, , ,
Production Method 17
- Synthetic method and application of 3-benzyl-1,3-thiazole-2-thioketone, China, , ,
Production Method 18
- Synthesis and biological activity of novel 2-thiazolidinone sulfonylurea derivativesChen, Qing-wu; Shen, De-long, Zhejiang Gongye Daxue Xuebao, 2008, 36(5), 562-564
Production Method 19
- Formation and transformation of esters. LVI. Effect of sulfuric acid on amino alcoholsCherbuliez, Emile; Chapalay, C.; Colak-Antic, Sl.; Marszalek, J.; Vallet, L.; et al, Helvetica Chimica Acta, 1964, 47(7), 2106-12
Production Method 20
- Circulating method for producing taurine from ethanolamine, China, , ,
2-Aminoethyl hydrogen sulfate Raw materials
2-Aminoethyl hydrogen sulfate Preparation Products
2-Aminoethyl hydrogen sulfate Related Literature
-
Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
-
Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
-
Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
Related Categories
- Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Organic sulfuric acids and derivatives Sulfuric acid monoesters
- Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Organic sulfuric acids and derivatives Sulfuric acid esters Sulfuric acid monoesters
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