Butyric acid - AR, ≥99% , CAS No.107-92-6

Name: Butyric acid - AR, ≥99% , CAS No.107-92-6
Brand: Aladdin Scientific
SKU: B110440
Availability: InStock

CAS: 107-92-6 Cat. No.: B110440 Summenformel: C₄H₈O₂ Molekulargewicht: 88.11 Beilstein Registry Number: 2264 EG-Nummer: 203-532-3

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QUALITÄT & REINHEIT AR ? ≥99%

Synonyms

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Warum diese Qualität

AR, ≥99% AR für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Literaturbeleg

In 448 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

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Synonyme

Spezifikationen & Reinheit

AR, ≥99%

Storage

Room temperature

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Note

Reinheit

≥99%

Namen und Kennungen

Pubchem Sid

508813768

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508813768

Kanonisches Lächeln

CCCC(=O)O

IUPAC Name

butanoic acid

InChIKey

FERIUCNNQQJTOY-UHFFFAOYSA-N

INCHI

1S/C4H8O2/c1-2-3-4(5)6/h2-3H2,1H3,(H,5,6)

Isomere SMILES

CCCC(=O)O

WGK Deutschland

RTECS

ES5425000

UN-Nummer

2820

Verpackungsgruppe

III

Molekulargewicht

88.11

Beilstein

2264

Reaxy-Rn

906770

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=906770&ln=

Dokumentation

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Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Klasse Fatty Acyls
    - Subclass Fatty acids and conjugates

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Klasse	Fatty Acyls
Subclass	Fatty acids and conjugates
Intermediate Tree Nodes	Not available
Direct Parent	Straight chain fatty acids
Alternative Parents	Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Straight chain fatty acid - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as straight chain fatty acids. These are fatty acids with a straight aliphatic chain.
External Descriptors	Straight chain fatty acids
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

3D-Struktur

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HCAR2 Tclin Hydroxycarboxylic acid receptor 2 (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

HDAC1 Tclin Histone deacetylase 1 (1 Activities)

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HDAC2 Tclin Histone deacetylase 2 (1 Activities)

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HDAC8 Tclin Histone deacetylase 8 (1 Activities)

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HDAC3 Tclin Histone deacetylase 3 (1 Activities)

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HDAC8 Tclin Histone deacetylase 8 (4516 Activities)

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

HDAC2 Tclin Histone deacetylase 2 (3971 Activities)

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HDAC3 Tclin Histone deacetylase 3 (3654 Activities)

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HDAC4 Tclin Histone deacetylase 4 (2328 Activities)

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HDAC9 Tclin Histone deacetylase 9 (708 Activities)

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HDAC7 Tclin Histone deacetylase 7 (1047 Activities)

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DCXR Tbio L-xylulose reductase (11 Activities)

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Caco-2 (12174 Activities)

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HL-60 (67320 Activities)

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K562 (73714 Activities)

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U-251 (51189 Activities)

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MIA PaCa-2 (5949 Activities)

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SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)

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FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)

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UGT1A8 Tbio UDP-glucuronosyltransferase 1-8 (233 Activities)

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UGT1A10 Tbio UDP-glucuronosyltransferase 1-10 (257 Activities)

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Hdac1 Histone deacetylase 1 (93 Activities)

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Hdac5 Histone deacetylase 5 (5 Activities)

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Hdac6 Histone deacetylase 6 (222 Activities)

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Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)

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HD1 Histone deacetylase (38 Activities)

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Meloidogyne incognita (862 Activities)

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Mus musculus (284745 Activities)

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Rattus norvegicus (775804 Activities)

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WEHI (120 Activities)

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3LLD122 (4 Activities)

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B16-F10 (4610 Activities)

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Radish (446 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Slc22a20 Solute carrier family 22 member 20 (86 Activities)

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

Slc22a6 Solute carrier family 22 member 6 (141 Activities)

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

Lolium rigidum (323 Activities)

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SARS-CoV-2 (38078 Activities)

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Wirkungsmechanismen

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)

C of A & Other Certificates(BSE/TSE, COO):

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8 results found

Lot Number	Certificate Type	Datum	Artikel
H2603124	Certificate of Analysis	Aug 04, 2026	B110440
B2518156	Certificate of Analysis	Feb 28, 2025	B110440
J2313555	Certificate of Analysis	Oct 24, 2023	B110440
H2317100	Certificate of Analysis	Aug 21, 2023	B110440
H2317099	Certificate of Analysis	Aug 21, 2023	B110440
J2215021	Certificate of Analysis	Oct 19, 2022	B110440
I2226203	Certificate of Analysis	Sep 30, 2022	B110440
H2231014	Certificate of Analysis	Sep 01, 2022	B110440

Chemische und physikalische Eigenschaften

Löslichkeit	It is miscible with water and can be mixed with ethanol and ether.
Empfindlichkeit	Moisture sensitive.
Brechungsindex	1.3965-1.3995
Flammpunkt (°F)	161 °F
Flammpunkt (°C)	72℃
Siedepunkt (°C)	162-165°C
Schmelzpunkt (°C)	-7--5°C
Molekulargewicht	88.110 g/mol
XLogP3	0.800
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	2
Exact Mass	88.0524 Da
Monoisotopic Mass	88.0524 Da
Topological Polar Surface Area	37.300 Å²
Heavy Atom Count	6
Formal Charge	0
Complexity	49.500
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

FAQs und Artikel

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Sources, Host-Regulatory Mechanisms, and Tumor-Immune Effects of Gut Microbiota-Derived Metabolites

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Butyric acid - AR, ≥99% , CAS No.107-92-6

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Butyric acid - AR, ≥99% , CAS No.107-92-6

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