Butyl glycolate - ≥98% , CAS No.7397-62-8

CAS: 7397-62-8 Cat. No.: B493056 Peso molecular: 132.16 Beilstein Registry Number: 1749477 Número EC: 230-991-7
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
AKOS009157665 | 3-FLUOROPYRIDINE-5-METHANOL | n-butyl hydroxyacetate | Butyl hydroxyacetate | 3H5QAS0HZX | NCGC00256074-01 | DTXCID4024725 | Acetic acid, 2-hydroxy-, butyl ester | 2H-Indol-2-one, 5-chloro-1,3-dihydro- | Butyl glycollate | Q27257204 | SY10
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25ml
B493056-25ml
9

21,90US$

35,90US$
Guardar 14,00 US$ (39.00%)
100ml
B493056-100ml
10

57,90US$

86,90US$
Guardar 29,00 US$ (33.37%)
500ml
B493056-500ml
2

253,90US$

296,90US$
Guardar 43,00 US$ (14.48%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Butyl glycolate is a glycolic acid derivative.
Butyl glycolate may be used in the preparation of N-(α-hydroxyacetyl)-(S)-isoleucine.

Specifications

Sinónimos
AKOS009157665 | 3-FLUOROPYRIDINE-5-METHANOL | n-butyl hydroxyacetate | Butyl hydroxyacetate | 3H5QAS0HZX | NCGC00256074-01 | DTXCID4024725 | Acetic acid, 2-hydroxy-, butyl ester | 2H-Indol-2-one, 5-chloro-1, 3-dihydro- | Butyl glycollate | Q27257204 | SY10
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504755561
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504755561
Sonrisas canónicasCCCCOC(=O)CO
IUPAC Namebutyl 2-hydroxyacetate
InChIKeyVFGRALUHHHDIQI-UHFFFAOYSA-N
INCHI1S/C6H12O3/c1-2-3-4-9-6(8)5-7/h7H,2-5H2,1H3
Isómeros SMILES CCCCOC(=O)CO
WGK Alemania 1
Peso molecular 132.16
Beilstein 1749477
Reaxy-Rn 1749477
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1749477&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic acids and derivatives
SubclassCarboxylic acid derivatives
Intermediate Tree Nodes Not available
Direct ParentCarboxylic acid esters
Alternative Parents Monocarboxylic acids and derivatives  Primary alcohols  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Carboxylic acid ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
DescripciónThis 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 Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

6 results found

Lot NumberCertificate TypeFechaArticulo
J2211404Certificate of AnalysisApr 03, 2026 B493056
J2211405Certificate of AnalysisApr 03, 2026 B493056
J2211406Certificate of AnalysisApr 03, 2026 B493056
J2211407Certificate of AnalysisApr 03, 2026 B493056
C2320609Certificate of AnalysisJan 09, 2025 B493056
C2320613Certificate of AnalysisOct 18, 2022 B493056
Propiedades químicas y físicas
Índice de refracción1.427
Punto de inflamación (°F)165.2 °F
Punto de inflamación (°C)74 °C
Punto de ebullición (°C)187-190 °C
Peso molecular132.160 g/mol
XLogP30.700
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count5
Exact Mass132.079 Da
Monoisotopic Mass132.079 Da
Topological Polar Surface Area46.500 Ų
Heavy Atom Count9
Formal Charge0
Complexity80.400
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Suling Zhang, Qi You, Xiaocong Zhuo, Zijie Shi, Weixuan Yao, Ting Lü, Dong Zhang.  (2023)  Rapid and simple determination of organophosphorus pesticides in urine using polydopamine-modified monolithic spin column extraction combined with liquid chromatography–mass spectrometry.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:37028207] [10.1016/j.chroma.2023.463959]
2. Han Yan, Xin Shu, Dongliang Zhou, Yong Yang, Lu Chen, Qianping Ran.  (2022)  Durability Improvement of Cement Using Amphiphilic Calcium Carbonate Nanoparticles.  Coatings,  12  (10): (1431).  [PMID:] [10.3390/coatings12101431]
3. Jiangdong Dai, Yongli Zou, Zhiping Zhou, Xiaohui Dai, Jianming Pan, Ping Yu, Tianbian Zou, Yongsheng Yan, Chunxiang Li.  (2013)  Narrowly dispersed imprinted microspheres with hydrophilic polymer brushes for the selective removal of sulfamethazine.  RSC Advances,  (4): (1965-1973).  [PMID:] [10.1039/C3RA44602F]
4. Jérémie Courtois, Heping Jin, Hongyu Chen, Hongping Zhang, Wei Feng.  (2024)  Superparamagnetic iron oxide nanoparticles functionalized with on-demand redox-responsive contractible coordination polymer brush as molecular actuator driven by π-dimerization.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2024.126303]
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