(-)-Ethyl L-lactate - photoresist grade, ≥99% , CAS No.687-47-8

CAS: 687-47-8 Cat. No.: E104553 Formula: C₅H₁₀O₃ Peso molecolare: 118.13 Beilstein Registry Number: 1720839 Numero EC: 211-694-1

GRADE & PURITY Photoresist grade, ≥99%

Synonyms

(L)-ethyl lactate | (S)-ethyl 2-hydroxypropanoate | ETHYL LACTATE, S- | NCGC00357157-01 | ETHYL LACTATE NATURAL | Propanoic acid, 2-hydroxy-, ethyl ester, (2S)- | (-)-ETHYL 2-HYDROXYPROPIONATE | DTXCID7022336 | L-(+)-lactic acid ethyl ester | ethyl (2S)-2

Storage

Room temperature

Shipped In

Normal

Specifications

Sinonimi

(L)-ethyl lactate | (S)-ethyl 2-hydroxypropanoate | ETHYL LACTATE, S- | NCGC00357157-01 | ETHYL LACTATE NATURAL | Propanoic acid, 2-hydroxy-, ethyl ester, (2S)- | (-)-ETHYL 2-HYDROXYPROPIONATE | DTXCID7022336 | L-(+)-lactic acid ethyl ester | ethyl (2S)-2

Specifiche e purezza

photoresist grade, ≥99%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Grado

Grado fotoresistente

Purezza

≥99%

Nomi e identificatori

Pubchem Sid

508806391

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508806391

Sorrisi canonici

CCOC(=O)C(C)O

IUPAC Name

ethyl (2S)-2-hydroxypropanoate

InChIKey

LZCLXQDLBQLTDK-BYPYZUCNSA-N

INCHI

1S/C5H10O3/c1-3-8-5(7)4(2)6/h4,6H,3H2,1-2H3/t4-/m0/s1

Isomeri SMILES

CCOC(=O)[C@H](C)O

WGK Germania

1

Numero UN

1192

Peso molecolare

118.13

Beilstein

1720839

Reaxy-Rn

1209448

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1209448&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acid esters
• Alternative Parents: Secondary alcohols Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary alcohol - Carboxylic acid ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as carboxylic acid esters. These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group).
• External Descriptors: ethyl 2-hydroxypropanoate

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

Proprietà chimiche e fisiche

• Indice di rifrazione: 1.413
• Rotazione specifica [α]: -10.8 ° (neat)
• Punto di infiammabilità (°F): 46℃
• Punto di infiammabilità (°C): 46℃
• Punto di ebollizione (°C): 154°C
• Punto di fusione (°C): -26°C
• Peso molecolare: 118.130 g/mol
• XLogP3: 0.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 118.063 Da
• Monoisotopic Mass: 118.063 Da
• Topological Polar Surface Area: 46.500 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 79.700
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• 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