Hypotaurine - CAS 300-84-5

Catalog:	BB020440
Product Name:	Hypotaurine
CAS:	300-84-5
Synonyms:	2-aminoethanesulfinic acid
Application:	Antioxidants

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	2-aminoethanesulfinic acid
Description:	Hypotaurine is an endogenous inhibitory amino acid for glycine receptor (GlyR). It acts as an antioxidant and a protective agent under physiological conditions.
Molecular Weight:	109.15
Molecular Formula:	C2H7NO2S
Canonical SMILES:	C(CS(=O)O)N
InChI:	InChI=1S/C2H7NO2S/c3-1-2-6(4)5/h1-3H2,(H,4,5)
InChI Key:	VVIUBCNYACGLLV-UHFFFAOYSA-N
Boiling Point:	354.9 °C at 760 mmHg
Flash Point:	168.5°C
Density:	1.511 g/cm³
Appearance:	Solid
MDL:	MFCD00038197
LogP:	0.73280

Publication Number	Title	Priority Date
CN-113249305-A	Oocyte in-vitro maturation culture solution additive, culture solution and application thereof	20210604
CN-113358783-A	Application of mogroside V and biomarker acting on pulmonary inflammation	20210604
CN-113416737-A	Grape hydrogen peroxide receptor gene and its coding protein and application	20210601
CN-113215087-A	Method for improving in-vitro maturation development rate of porcine oocytes by adopting agomelatine	20210531
CN-113186189-A	gRNA for knocking out pig NPHS2 gene and related application thereof	20210519

PMID	Publication Date	Title	Journal
31926187	20200215	Identification of key metabolites during cisplatin-induced acute kidney injury using an HPLC-TOF/MS-based non-targeted urine and kidney metabolomics approach in rats	Toxicology
31626840	20200101	Metabolomic-transcriptomic landscape of 8-epidiosbulbin E acetate -a major diterpenoid lactone from Dioscorea bulbifera tuber induces hepatotoxicity	Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association
23665415	20130705	Alterations in hepatic metabolism of sulfur amino acids in non-obese type-2 diabetic Goto-Kakizaki rats	Chemico-biological interactions
23603744	20130601	Paracoccus denitrificans PD1222 utilizes hypotaurine via transamination followed by spontaneous desulfination to yield acetaldehyde and, finally, acetate for growth	Journal of bacteriology
23020609	20121019	Biomimetic synthesis of the apoptosis-inducing thiazinoquinone thiaplidiaquinone A	The Journal of organic chemistry

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Related Functional Groups

Sulfur Compounds

[518012-62-9]
[2-[2-(2-Methoxyethoxy)ethoxy]ethoxy]p-toluenesulfonate
[2006276-82-8]
[3-(N,N-Dimethylsulfamoyl)phenyl]methanesulfonyl Chloride
[1866059-82-6]
1,1,2,2-Tetrafluoro-3-methylsulfonylpropane
[6633-90-5]
1,4-Butanedithiol diacetate
[85-47-2]
1-Naphthalenesulfonic acid
[832739-83-0]
3-[(4-Chlorophenyl)sulfonyl]-5-methoxyaniline

GHS Hazard Statement:	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
Precautionary Statement:	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

Complexity:	55.5
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	109.01974964
Formal Charge:	0
Heavy Atom Count:	6
Hydrogen Bond Acceptor Count:	4
Hydrogen Bond Donor Count:	2
Isotope Atom Count:	0
Monoisotopic Mass:	109.01974964
Rotatable Bond Count:	2
Topological Polar Surface Area:	82.5 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	-1.5