(±)-1,3-Butanediol - Anhydrous Grade, ≥99% , CAS No.107-88-0

CAS: 107-88-0 Cat. No.: B119672 Fórmula: C4H10O2 Peso molecular: 90.12 Beilstein Registry Number: 1731276 Número CE: 203-529-7
Disponível para encomenda
GRAU & PUREZA Anhydrous Grade ? Anhydrous grade — water removed and packaged dry for moisture-sensitive chemistry. Use in reactions where even trace water would interfere or quench. ≥99%
Synonyms
1,3-BUTYLENE GLYCOL [FCC] | ShiZhenTaiYiTang Moxibustion Patch | .beta.-Butylene glycol | 1,3-Butylene glycol | AI3-11077 | F8880-3340 | FT-0605126 | (R)-1,3-butanediol | 1,3-butane diol | 1,3-Butanodiol | AKOS000119043 | B0679 | BUTANEDIOL,1,3- | BUTYLEN
Storage
Room temperature,Argon charged
Shipped In
Normal
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Tamanho
USA
Alemanha (EU)*
Preço
Qtd
100ml
B119672-100ml
1 Em stock
—
45,90US$
500ml
B119672-500ml
1 Em stock
1 Em stock
99,90US$
Enter a quantity for the sizes you want to add.
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Por que este grau

Anhydrous Grade, ≥99% Anhydrous Grade para fluxos de trabalho cromatográficos e analíticos sensíveis que exigem interferência mínima da linha de base.

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Armazenamento e envio

Room temperature,Argon charged Envio Normal. Consulte o COA específico do lote para obter as especificações exatas.

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Documentos de qualidade

SDS, COA, ficha técnica e folha de especificações disponíveis para download. COA específico do lote acessível por meio de pesquisa por número de lote.

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Comprovação documental

Citado em 39 publicações revisadas por pares nas áreas de cromatografia, síntese orgânica e reações de acoplamento cruzado.

Visão geral

A building block for proteomics research


application:

(±)-1,3-Butanediol may be used as a solvent in the preparation of 6-methoxy-2-benzoxazolinone via condensation reaction between 2-hydroxy-4-methoxyphenyJarnmonium chloride and urea. It can also react with carboxylic acids to form the corresponding chlorohydrin esters in the presence of chlorotrimethylsilane.


Especificações

Sinónimos
1,3-BUTYLENE GLYCOL [FCC] | ShiZhenTaiYiTang Moxibustion Patch | .beta.-Butylene glycol | 1,3-Butylene glycol | AI3-11077 | F8880-3340 | FT-0605126 | (R)-1,3-butanediol | 1,3-butane diol | 1,3-Butanodiol | AKOS000119043 | B0679 | BUTANEDIOL,1,3- | BUTYLEN
Especificações e pureza
Anhydrous Grade, ≥99%
Condições de armazenamento de armazenamento
Room temperature,Argon charged
Enviado em
Normal
Grau
Anhydrous Grade
Pureza
≥99%
Nomes e identificadores
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/528753707
Sorrisos canónicos
CC(CCO)O
IUPAC Name
butane-1,3-diol
InChIKey
PUPZLCDOIYMWBV-UHFFFAOYSA-N
INCHI
1S/C4H10O2/c1-4(6)2-3-5/h4-6H,2-3H2,1H3
SMILES isoméricas
CC(CCO)O
WGK Alemanha
1
RTECS
EK0440000
Peso molecular
90.12
Beilstein
1731276
Reaxy-Rn
1718945
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1718945&ln=

Documentação

📋 Ficha de dados de segurança (FDS)

Documento abrangente sobre perigos, manuseamento, armazenamento e conformidade regulamentar.

<<<<<<< HEAD Baixar SDS → ======= Baixar SDS → >>>>>>> release248-p3

✅ Certificado de análise (COA)

Dados de qualidade específicos do lote. Introduza o número de lote para obter o COA exato.

Consultar COA →

📊 Ficha técnica

Resumo de referência rápida das especificações e aplicações do produto.

Ver ficha técnica →

🔬 Folha de especificações

Atributos de qualidade completos e critérios de aceitação para este grau.

Ver folha de especificações →

Dados avançados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClasseOrganooxygen compounds
SubclassAlcohols and polyols
Intermediate Tree Nodes Not available
Direct ParentSecondary alcohols
Alternative Parents Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Secondary alcohol - Hydrocarbon derivative - Primary alcohol - Aliphatic acyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as secondary alcohols. These are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl).
External Descriptors a glycol
Estrutura 3D
Modelo de Estrutura Química Interativa





Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
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.

16 results found

Lot NumberCertificate TypeDataItem
C2617299C2617299Certificate of AnalysisMar 11, 2026 B119672
C2617300C2617300Certificate of AnalysisMar 11, 2026 B119672
C2617301C2617301Certificate of AnalysisMar 11, 2026 B119672
B2525152B2525152Certificate of AnalysisFeb 18, 2025 B119672
B2525153B2525153Certificate of AnalysisFeb 18, 2025 B119672
B2525155B2525155Certificate of AnalysisFeb 18, 2025 B119672
E2523076E2523076Certificate of AnalysisFeb 18, 2025 B119672
B2506097B2506097Certificate of AnalysisMar 26, 2024 B119672
D2411158D2411158Certificate of AnalysisMar 26, 2024 B119672
D2411159D2411159Certificate of AnalysisMar 26, 2024 B119672
D2411160D2411160Certificate of AnalysisMar 26, 2024 B119672
B2428020B2428020Certificate of AnalysisMar 31, 2023 B119672
B2428188B2428188Certificate of AnalysisMar 31, 2023 B119672
D2308759D2308759Certificate of AnalysisMar 31, 2023 B119672
D2308765D2308765Certificate of AnalysisMar 31, 2023 B119672
D2308766D2308766Certificate of AnalysisMar 31, 2023 B119672
Propriedades químicas e físicas
SolubilidadeSolubility in water: soluble Solubility in other solvents: soluble in acetone, methyl ethyl ketone, ethanol slightly soluble in ether practically insoluble in aliphatic hydrocarbons, benzene, toluene and CCl4.
SensibilidadeMoisture sensitive
Índice de refração1.44
Ponto de inflamação (°F)251.6℉
Ponto de inflamação (°C)122℃
Ponto de ebulição (°C)207°C
Ponto de fusão (°C)-50℃
Peso molecular90.120 g/mol
XLogP3-0.400
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass90.0681 Da
Monoisotopic Mass90.0681 Da
Topological Polar Surface Area40.500 Ų
Heavy Atom Count6
Formal Charge0
Complexity28.700
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQs e artigos
The Guide to Anhydrous Grade for Reagents
Solvents, Co-solvents, and Solubilization Systems in Home and Personal Care Formulations: Classification, Functions, and Selection Guide
From Structure to Rheology: How Carbomer Forms Gel Structures and Enables Thickening, Suspension, and Auxiliary Emulsion Stabilization
Why Do Alcohols Differ in Function: Why Is Glycerol Mainly Moisturizing, Propylene Glycol Mainly Solubilizing, and Isopropyl Alcohol Fast-Drying? — Understanding Personal Care Formulation Functions from Structural Differences
Thickening, Suspension, Auxiliary Stabilization, and Agglomeration Mechanisms of Xanthan Gum in Personal Care Formulations: From Molecular Structure to Processing Applications
Analysis of Structural Differences in Diols: Moisturization, Co-solvency, Skin Feel, and Formulation Selection for Propylene Glycol, Butylene Glycol, and Medium- to Long-Chain 1,2-Alkanediols
Analysis of Hydrolyzed Pearl as a Cosmetic Raw Material: Preparation Process, Active Components, and Skincare Formulation Applications
Antioxidant Mechanisms of Ferulic Acid in Skincare, Vitamin C/E Synergy, and Stable Delivery Applications
Moisturizing Mechanism of Polyglutamic Acid: From the γ-Glutamyl Structure to Hydration Networks and Surface Film-Forming Behavior
Moisturizing Mechanisms of Tremella fuciformis Polysaccharides: From Polysaccharide Structure and Hydration Rheology to Dynamic Film Formation on the Skin Surface
How Arbutin Regulates Melanin Production: α/β Anomeric Configuration and Tyrosinase Action
Rotary-Evaporation-Assisted Reversible Dehydration Reactions: Reduced-Pressure Evaporation, Removal of Volatile Components, and Equilibrium Response
Citations of This Product
Calculadoras de soluções
Revisões

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