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Tiglic acid

Tiglic acid Structure
CAS No.
80-59-1
Chemical Name:
Tiglic acid
Synonyms
(E)-2-Methylbut-2-enoic acid;tiglic;2-METHYL-2-BUTENOIC ACID;2-METHYLBUT-2-ENOIC ACID;(E)-2-METHYL-2-BUTENOIC ACID;TRANS-2,3-DIMETHYLACRYLIC ACID;NSC 8999;iglicaci;FEMA 3599;NSC 44235
CBNumber:
CB4199986
Molecular Formula:
C5H8O2
Molecular Weight:
100.12
MOL File:
80-59-1.mol
MSDS File:
SDS
Modify Date:
2024/6/4 19:18:49

Tiglic acid Properties

Melting point 61-64 °C(lit.)
Boiling point 95-96 °C12 mm Hg(lit.)
Density 0.969 g/mL at 25 °C(lit.)
FEMA 3599 | 2-METHYL-TRANS-2-BUTENOIC ACID
refractive index nD81 1.4342
Flash point 101°C
storage temp. 2-8°C
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form Crystalline Powder and Chunks
pka pK (25°) 5.02
Specific Gravity 0.969
color White to beige
Odor at 10.00 % in dipropylene glycol. sweet dry spicy woody caramel
Odor Type spicy
Water Solubility SOLUBLE IN HOT WATER
JECFA Number 1205
Merck 14,9433
BRN 1236500
InChIKey UIERETOOQGIECD-ONEGZZNKSA-N
LogP 1.35
CAS DataBase Reference 80-59-1(CAS DataBase Reference)
NIST Chemistry Reference 2-Butenoic acid, 2-methyl-, (E)-(80-59-1)
EPA Substance Registry System 2-Butenoic acid, 2-methyl-, (2E)- (80-59-1)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  C,Xi
Risk Statements  34-36/37/38
Safety Statements  26-36/37/39-45-24/25-27
RIDADR  UN 3261 8/PG 2
WGK Germany  2
RTECS  GQ5430000
TSCA  Yes
HazardClass  8
PackingGroup  III
HS Code  29161980
NFPA 704
0
2 0

Tiglic acid price More Price(9)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) W359904 trans-2-Methyl-2-butenoic acid ≥99%, FG 80-59-1 1SAMPLE-K ₹5141.88 2022-06-14 Buy
Sigma-Aldrich(India) W359904 trans-2-Methyl-2-butenoic acid ≥99%, FG 80-59-1 100G ₹9114.65 2022-06-14 Buy
Sigma-Aldrich(India) W359904 trans-2-Methyl-2-butenoic acid ≥99%, FG 80-59-1 1KG ₹20675.75 2022-06-14 Buy
Sigma-Aldrich(India) T35203 trans-2,3-Dimethylacrylic acid 98% 80-59-1 100G ₹6776.45 2022-06-14 Buy
TCI Chemicals (India) T0246 Tiglic Acid min. 98.0 % 80-59-1 25G ₹2800 2022-05-26 Buy
Product number Packaging Price Buy
W359904 1SAMPLE-K ₹5141.88 Buy
W359904 100G ₹9114.65 Buy
W359904 1KG ₹20675.75 Buy
T35203 100G ₹6776.45 Buy
T0246 25G ₹2800 Buy

Tiglic acid Chemical Properties,Uses,Production

Description

frarc.s-2-Methyl-2-butenoic acid has a sweet, warm, spicy odor. May be synthesized from 2-hydroxy-2-methylbutyronitrile.

Chemical Properties

WHITE TO BEIGE CRYSTALLINE POWDER AND CHUNKS

Occurrence

Reported found in celery leaves and stalk, cocoa, mango, dried bonito and Roman chamomile oil

Uses

Tiglic acid is the stable isomer of angelic acid. Tiglic acid was found as glyceride in croton oil, as butyl ester in the oil of the Roman camomile, and as geranyl tiglate in oil of geranium. Tiglic a cid is formed during the charcoaling of maple wood.

Definition

ChEBI: A 2-methylbut-2-enoic acid having its double bond in trans-configuration.

General Description

A white lustrous flaked solid with a fruity or spicy odor. About the same density as water and slightly soluble in water. May burn if heated to high temperatures. May severely irritate skin, eyes, lungs or mucous membranes.

Air & Water Reactions

Slightly soluble in water.

Reactivity Profile

TIGLIC ACID is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in Tiglic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.

Health Hazard

TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.

Safety Profile

Low toxicity by ingestion and skin contact. A severe skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.

Purification Methods

Crystallise it from water. It is steam volatile and is soluble in organic solvents. [Beilstein 2 IV 1552.]

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E-2,3-DIMETHYLACRYLIC ACID FEMA 3599 trans-2,3-Dimethylacrylic acid~(E)-2-Methyl-2-butenoic acid TRANS-2-METHYL-2-BUTENOIC ACID 99+% TiglicAcid,>98% trans-2-Methyl-2-butenoicacid,97% 2-Butenoicacid,2-methyl-,(E)- 2-methyl-(E)-2-butenoic acid 2-methyl-,(E)-2-Butenoicacid Cevadic acid cevadicacid Crotonic acid, 2-methyl-, (E)- Crotonicacid,2-methyl-,(E)- crotonolicacid Tiglic acid, E tiglicacid,[corrosivesolid] Tiglinic acid tiglinicacid Tiglinsαure trans-2,3-Dimethylacrylsαure trans-2-Methyl-2-butensαure trans-2-methyl-but-2-enoicacid trans-2-Methylcrotonsαure trans-α,β-Dimethylacrylicacid TIGLIC ACID(RG) (E)-2-Methylbut-2-ensure TIGLINSAEURE alpha-Methylcrotonic acid TRANS-2,3-DIMETHYLACRYLIC ACID (TIGLIC ACID) TRANS-A,B-DIMETHYLACRYLIC ACID trans-2,3-Dimethylacrylic acid, trans-2-Methyl-2-butenoic acid trans-2,3-Dimethylacrylic acid, trans-2-Methyl-2-butenoic acid, Tiglic acid 2,3-DIMETHYLACRYLIC ACID 2-METHYL-TRANS-2-BUTENOIC ACID 2-METHYLCROTONIC ACID TRANS-ALPHA,BETA-DIMETHYLACRYLIC ACID TRANS-2-METHYL-2-BUTENOIC ACID TRANS-2-METHYLCROTONIC ACID RARECHEM AL BO 0403 TIGLIC ACID (E)-2-Methyl-2-butensαure (E)-2-Methylcrotonic acid (e)-2-methylcrotonicacid (E)-2-Methylcrotonsαure (E)-α-Methylcrotonicacid 2-Butenoicacid,2-methyl-,(2E)- trans-2,3-Dimethylacrylic acid,98% trans-2,3-DiMethylacrylic acid, 98% 100GR NSC 44235 NSC 8999 trans-2-Methyl-2 (E)-2-Methyl-2-butenoic Acid 2-Methylcrotonic Acid trans-2,3-Dimethylacrylic acid 98% Tiglic acid (C5H8O2) trans-2,3-DIMETHYLACRYLIC ACID Extra Pure (E)-tiglic acid Tiglic acid USP/EP/BP iglicaci