Sorbic acid ≥99.0% | Sigma-Aldrich

Properties

Related Categories	Antibiotics, Antibiotics A to Z, Antibiotics N-S, Antibiotics by Application, Antifungal, Biochemicals and Reagents, Fatty Acids and conjugates, Fatty Acyls, Lipids, Others, Polyunsaturated, Preservatives and Disinfectants, Spectrum of Activity, Unsaturated Fatty Acids and Derivatives More...
vapor pressure	0.01 mmHg ( 20 °C)
assay	≥99.0%
mp	132-135 °C(lit.)
storage temp.	2-8°C

Description

Packaging

100, 250, 500 g in poly bottle

Biochem/physiol Actions

Sorbic acid can be used to inhibit bacterial, yeast and fungal sulfhydryl enzymes by inhibiting amino acid uptake.

Price and Availability

Related Papers

Quantitative structure-activity relationship studies for prediction of antimicrobial activity of synthesized 2,4-hexadienoic acid derivatives. Balasubramanian Narasimhan et al Bioorg. Med. Chem. Lett. 17, 5836-45, (2007)

Documents

Certificate of Analysis

Certificate of Origin

FT-IR Raman

FT-NMR

Safety Information

Symbol	GHS07
Signal word	Warning
Hazard statements	H315-H319-H335
Precautionary statements	P261-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes (Europe)	Xi
Risk Statements (Europe)	36/37/38
Safety Statements (Europe)	26
WGK Germany	1
RTECS	WG2100000
Flash Point(F)	260.6 °F
Flash Point(C)	127 °C

Technical information & documentation associated with this product is available in the Safety & Documentation tab.

Papers

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Quantitative structure-activity relationship studies for prediction of antimicrobial activity of synthesized 2,4-hexadienoic acid derivatives. Balasubramanian Narasimhan et al Bioorg. Med. Chem. Lett. 17, 5836-45, (2007)

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Molecular modifications on carboxylic acid derivatives as potent histone deacetylase inhibitors: Activity and docking studies. Gamze Bora-Tatar et al Bioorg. Med. Chem. 17, 5219-28, (2009)

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Contribution of cinnamic acid analogues in rosmarinic acid to inhibition of snake venom induced hemorrhage. Hnin Thanda Aung et al Bioorg. Med. Chem. 19, 2392-6, (2011)

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Merck 14,8721

Beil. 2,IV,1701

Fieser 15,296

Aldrich MSDS 1, 1021:D / Corp MSDS 1 (1), 1844:C / FT-IR 1 (1), 502:A / FT-IR 2 (1), 785:B / FT-NMR 1 (1), 784:C / IR-Spectra (2), 265:E / IR-Spectra (3), 294:F / NMR-Reference 2 (1), 438:B / RegBook 1 (1), 551:E / Sax 6, 2459 / Sigma FT-IR 1 (1), 712:A / Structure Index 1, 78:C:3 / Vapor Phase 3, 588:D