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Formamidinesulfinic acid - 98%, high purity , CAS No.1758-73-2

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Formamidinesulfinic acid - 98%, high purity , CAS No.1758-73-2

11 Citations

COA

Grade & Purity:

≥98%

Cas Number: 1758-73-2
Molecular Weight: 108.12
Beilstein Registry Number: 506653
EC Number: 217-157-8
MDL number: MFCD00002397
PubChem CID: 61274

In stock

Item Number

T104705

Grouped product items
SKU	Size	Availability	Price
T104705-25g	25g	3	$14.90
T104705-100g	100g	3	$23.90
T104705-500g	500g	3	$43.90

View related series

Non heterocyclic block (8163) Sulfur containing compounds (986) Thiourea (9) ureas (94)

Basic Description

Synonyms	AMINOIMINOMETHANESULFINIC ACID \| Manofast \| NSC 226979 \| formamidine sulfuric acid \| Tox21_200647 \| A812126 \| Formamidinesulfinic acid, >=98% \| Methanesulfinic acid, aminoimino- \| Formamidinesulfinic acid \| EC 217-157-8 \| MFCD00002397 \| Formamidine sulfin
Specifications & Purity	≥98%
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Sulfinic acids and derivatives
    - Subclass Sulfinic acids

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Sulfinic acids and derivatives
Subclass	Sulfinic acids
Intermediate Tree Nodes	Not available
Direct Parent	Sulfinic acids
Alternative Parents	Carboximidamides Organosulfur compounds Organopnictogen compounds Organic oxides Imines Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Sulfinic acid - Carboximidamide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organonitrogen compound - Imine - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as sulfinic acids. These are compounds containing a sulfinic acid functional group, with the general structure RS(=O)OH (R = organyl, not H).
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	amino(imino)methanesulfinic acid
INCHI	InChI=1S/CH4N2O2S/c2-1(3)6(4)5/h(H3,2,3)(H,4,5)
InChIKey	FYOWZTWVYZOZSI-UHFFFAOYSA-N
Smiles	C(=N)(N)S(=O)O
Isomeric SMILES	C(=N)(N)S(=O)O
WGK Germany	1
RTECS	PB0372500
UN Number	3341
Packing Group	II
Molecular Weight	108.12
Beilstein	506653
Reaxy-Rn	506653

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

15 results found

Lot Number	Certificate Type	Date	Item
B2506592	Certificate of Analysis	Jan 10, 2025	T104705
B2506646	Certificate of Analysis	Jan 10, 2025	T104705
B2506647	Certificate of Analysis	Jan 10, 2025	T104705
B2506648	Certificate of Analysis	Jan 10, 2025	T104705
G2417476	Certificate of Analysis	Jun 13, 2024	T104705
A2506288	Certificate of Analysis	Dec 11, 2023	T104705
A2419684	Certificate of Analysis	Dec 11, 2023	T104705
A2419682	Certificate of Analysis	Dec 11, 2023	T104705
A2419683	Certificate of Analysis	Dec 11, 2023	T104705
A2304230	Certificate of Analysis	Jan 17, 2023	T104705
J2211210	Certificate of Analysis	Jul 22, 2022	T104705
H2316016	Certificate of Analysis	Jul 22, 2022	T104705
J2211208	Certificate of Analysis	Jul 22, 2022	T104705
J2211220	Certificate of Analysis	Jul 22, 2022	T104705
F2223132	Certificate of Analysis	Jun 29, 2022	T104705

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Chemical and Physical Properties

Solubility	Thiourea dioxide is sensitive to moisture. Immediately decompose in boiling water. In slightly alkaline solutions, it decomposes into urea and hyposulfuric acid. Easy to dissolve in water, the aqueous solution is slightly acidic, soluble in concentrated s
Sensitivity	Moisture & heat sensitive.
Melt Point(°C)	126°C
Molecular Weight	108.120 g/mol
XLogP3	-1.100
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	1
Exact Mass	107.999 Da
Monoisotopic Mass	107.999 Da
Topological Polar Surface Area	106.000 Å²
Heavy Atom Count	6
Formal Charge	0
Complexity	89.500
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Ning Zhang, Yujie Xu, Rongjin Shi, Man Zhou, Yuanyuan Yu, Ping Wang, Qiang Wang. (2024) Protein-based coating strategy for preparing durable sunlight-driven rechargeable antibacterial, super hydrophilic, and UV-resistant textiles. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 258 (128761).
2. Ning Zhang, Wenda Wang, Man Zhou, Yuanyuan Yu, Ping Wang, Qiang Wang. (2023) A controllable , universal, and natural supramolecular assembly coating strategy for multifunctionality textiles of antibacterial properties, UV resistance, antioxidant, and secondary reactivity. INDUSTRIAL CROPS AND PRODUCTS, 198 (116637).
3. Qishan Fu, Muzi Yang, Zhongfei Liu, Hao Yang, Fengquan She, Xiaoqi Zhang, Fangyan Xie, Yuwen Hu, Jian Chen. (2022) Unveiling the promotion of intermediates transport kinetics on the N/S co-doping 3D structure titanium carbide aerogel for high-performance supercapacitors. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 618 (161).
4. Ning Zhang, Zhicheng Deng, Qiang Wang, Man Zhou, Ping Wang, Yuanyuan Yu. (2022) Phase-transited lysozyme with secondary reactivity for moisture-permeable antibacterial wool fabric. CHEMICAL ENGINEERING JOURNAL, 432 (134198).
5. Xu Xiaozhi, Wang Jiajie, Zhou Awu, Dong Siyuan, Shi Kaiqiang, Li Biao, Han Jingbin, O’Hare Dermot. (2021) High-efficiency CO2 separation using hybrid LDH-polymer membranes. Nature Communications, 12 (1): (1-10).
6. Yuanyuan Ding, Jianhong Yang, Jun Cai. (2018) Preparation of guanidinylated carboxymethyl chitosan and its application in the diffusive gradients in thin films (DGT) technique for measuring labile trace metals in water. INTERNATIONAL JOURNAL OF ENVIRONMENTAL ANALYTICAL CHEMISTRY,
7. Yuanxiu Yang, Xinjiang Hu, Yunlin Zhao, Lihua Cui, Zhujian Huang, Jianliang Long, Jiawen Xu, Jianbin Deng, Cuiyu Wu, Wenwei Liao. (2017) Decontamination of tetracycline by thiourea-dioxide–reduced magnetic graphene oxide: Effects of pH, ionic strength, and humic acid concentration. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 495 (68).
8. Benqiao He, Yixuan Shao, Mengzhu Liang, Jianxin Li, Yu Cheng. (2015) Biodiesel production from soybean oil by guanidinylated chitosan. FUEL, 159 (33).
9. Zhihua Cui, Xin Li, Xidong Wang, Kemei Pei, Weiguo Chen. (2013) Structure and properties of N-heterocycle-containing benzotriazoles as UV absorbers. JOURNAL OF MOLECULAR STRUCTURE, 1054-1055 (94).
10. Bopei Wei, Shuaihao Wang, Jiaxin Wang, Man Zhou, Ping Wang, Yuanyuan Yu, Qiang Wang. (2024) An eco-friendly, water-saving and cost-effective approach to manufacturing machine-washable wool fabric using a broad-temperature-range proteinase (BTRP) and an innovative “pad-steam-pad-cold batch” technique.. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 282 (136884).
11. Yueyue Wang, Pu Ma, Jun Huang, Lifang Guo, Yu Wang, Huamin Zhai, Hao Ren. (2024) Effect of Sheet Properties of Cellulosic Polyglycidyl Methacrylate-Grafted Fibers in a Cationic Polyacrylamide/SiO2/Anionic Polyacrylamide Retention Aid System. Polymers, 16 (12): (1678).

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