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T35203

Sigma-Aldrich

trans-2,3-Dimethylacrylic acid

98%

Synonym(s):

Tiglic acid, trans-2,3-Dimethylacrylic acid, trans-2-Methyl-2-butenoic acid

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About This Item

Linear Formula:
CH3CH=C(CH3)COOH
CAS Number:
80-59-1
Molecular Weight:
100.12
Beilstein:
1236500
EC Number:
201-295-0
MDL number:
MFCD00066864
UNSPSC Code:
12352100
PubChem Substance ID:
24900147
NACRES:
NA.22

Quality Level

200

Assay

98%

bp

95-96 °C/12 mmHg (lit.)

mp

61-64 °C (lit.)

density

0.969 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

C\C=C(/C)C(O)=O

InChI

1S/C5H8O2/c1-3-4(2)5(6)7/h3H,1-2H3,(H,6,7)/b4-3+

InChI key

UIERETOOQGIECD-ONEGZZNKSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

203.0 °F

Flash Point(C)

95 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Tigliane-type diterpene esters from Synadenium grantii.
R Bagavathi et al.
Planta medica, 54(6), 506-510 (1988-12-01)
Araceli Larios et al.
Applied microbiology and biotechnology, 65(4), 373-376 (2004-07-13)
Candida antarctica lipase fraction B (CAL-B) showed substrate specificity in the synthesis of esters in hexane involving reactions of short-chain acids having linear (acetic and butyric acids) and branched chain (isovaleric acid) structures, an unsaturated (tiglic acid) fatty acid, and
K D Santos et al.
International journal of immunopharmacology, 18(12), 761-769 (1996-12-01)
The present study was undertaken to assess the influence of 25 organic acids, which appear in high concentrations in tissues of patients with various organic acidaemias, on the proliferation of human peripheral lymphocytes stimulated with concanavalin A (Con A) (a
Susan Matthew et al.
Phytochemistry, 70(17-18), 2058-2063 (2009-10-10)
The Floridian marine cyanobacterium Lyngbya confervoides afforded cyclodepsipeptides, termed tiglicamides A-C (1-3), along with their previously reported analogues largamides A-C (4-6), all of which possess an unusual tiglic acid moiety. Their structures were deduced by one- and two-dimensional NMR combined
P F Schuck et al.
Neurochemistry international, 45(5), 661-667 (2004-07-06)
Accumulation of methylmalonic acid (MMA) in tissues and biological fluids is the biochemical hallmark of patients affected by the neurometabolic disorder known as methylmalonic acidemia (MMAemia). Although this disease is predominantly characterized by severe neurological findings, the underlying mechanisms of
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