T35203
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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100 G
₪517.00
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100 G
₪517.00
About This Item
Linear Formula:
CH3CH=C(CH3)COOH
CAS Number:
Molecular Weight:
100.12
Beilstein:
1236500
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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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Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
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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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
Tigliane-type diterpene esters from Synadenium grantii.
R Bagavathi et al.
Planta medica, 54(6), 506-510 (1988-12-01)
Araceli Larios et al.
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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
[Effects of a skin stimulating salve].
W RIESE
Wiener medizinische Wochenschrift (1946), 100(45-46), 758-759 (1950-11-25)
Y S Li et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 26(12), 835-837 (2003-06-05)
To study the chemical constituents of Ligularia vellerea. The compounds were isolated by column chromatography, and the structures were identified by NMR spectral data and other methods. Seven compounds were isolated and identified as 4-hydroxyacetophenone, 8 alpha-hydroxy-7(11)-eremophilen-12, 8 beta-olide, umbelliferone
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