3-Mercaptopropionic acid - Biochemical, ≥99% , CAS No.107-96-0

CAS: 107-96-0 Cat. No.: M103036 Formule: C₃H₆O₂S Poids moléculaire: 106.14 Beilstein Registry Number: 773807 Numéro CE: 203-537-0

QUALITÉ & PURETÉ Biochemical, ≥99%

Synonyms

Thiohydracrylic acid|3-Sulfanylpropanoic acid|ss--Mercaptopropanoic acid|3-Dimethylamino-2-methylpropylchloridehydrochloride|3 Mercaptopropionic Acid|3-MERCAPTOPROPIONIC ACID [HSDB]|3-thiohydracrylic acid|ss--Thiopropionic acid|beta-Thiopropionic acid|3-Thiopropionic acid|.beta.-Thiopropionic acid|Thiopropionic acid; 3-Thiopropanoic acid; beta-Mercaptopropionic acid|3-Mercaptopropanoic acid|3-mercapto-propanoic acid|Propionic acid, 3-mercapto-|Mercaptopropionic acid, 3-|3-Thiolpropanoic acid|ss--Mercaptopropionic acid|betamercaptopropionic acid|beta-Mercaptopropionic acid|2-Mercaptoethanecarboxylic acid|3-Thiopropanoic acid|Propionic acid, 3-mercpato-|3-MERCAPTOPROPIONIC ACID|3-mercapto-propionic acid|Hydracrylic acid, 3-thio-|.beta.-Mercaptopropanoic acid|.beta.-Mercaptopropionic acid|Propanoic acid, 3-mercapto-|MERCAPTOPROPIONIC ACID [INCI]|3-Sulfanylpropanoic acid #|beta-Mercaptopropanoic acid|3-Mercaptopropanoic acid, 9CI|3-Mercaptopropionicacid|DEAMINO CYSTEINE

Storage

Room temperature,Argon charged

Shipped In

Normal

Spécifications

Synonymes

Thiohydracrylic acid | 3-Sulfanylpropanoic acid | ss--Mercaptopropanoic acid | 3-Dimethylamino-2-methylpropylchloridehydrochloride | 3 Mercaptopropionic Acid | 3-MERCAPTOPROPIONIC ACID [HSDB] | 3-thiohydracrylic acid | ss--Thiopropionic acid | beta-Thiopropionic acid | 3-Thiopropionic acid | .beta.-Thiopropionic acid | Thiopropionic acid; Afficher plus

Spécifications et pureté

Biochemical, ≥99%

Conditions de stockage de stockage

Room temperature,Argon charged

Expédié en

Normal

Grade

Biochemical

Pureté

≥99%

Noms et identifiants

Pubchem Sid

508808833

Sourires canoniques

C(CS)C(=O)O

IUPAC Name

3-sulfanylpropanoic acid

InChIKey

DKIDEFUBRARXTE-UHFFFAOYSA-N

INCHI

1S/C3H6O2S/c4-3(5)1-2-6/h6H,1-2H2,(H,4,5)

Isomères SMILES

C(CS)C(=O)O

WGK Allemagne

1

RTECS

UF5270000

Numéro ONU

2922

Poids moléculaire

106.14

Beilstein

773807

Reaxy-Rn

773807

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=773807&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Carboxylic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acids
• Alternative Parents: Monocarboxylic acids and derivatives Alkylthiols Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Monocarboxylic acid or derivatives - Carboxylic acid - Alkylthiol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
• External Descriptors: mercaptopropanoic acid

Data sources

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

Cibles associées (humaines)

MMP3 Tchem Matrix metalloproteinase 3 (3433 Activities)

Discover Target: MMP3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cibles associées (non humaines)

blaZ Beta-lactamase (285 Activities)

Discover Target: blaZ

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Staphylococcus aureus (210822 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Escherichia coli (133304 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Haemophilus influenzae (8812 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Bacillus subtilis (32866 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Bacillus cereus (7522 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mus musculus (284745 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in water, soluble in ethanol, benzene, and ether.
• Sensibilité: Air Sensitive Hygroscopic
• Point de congélation (°C): 17 °C
• Indice de réfraction: 1.492
• Point d'éclair (°F): 200.1 °F
• Point d'éclair (°C): 93.4°C
• Point d'ébullition (°C): 110-111°C
• Point de fusion (°C): 15-18°C
• Poids moléculaire: 106.150 g/mol
• XLogP3: 0.400
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 106.009 Da
• Monoisotopic Mass: 106.009 Da
• Topological Polar Surface Area: 38.300 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 52.800
• 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