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About This Item
Linear Formula:
HOOCCH=CHCOOH
CAS Number:
Molecular Weight:
116.07
FEMA Number:
2488
Council of Europe no.:
25
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
8.025
EC Number:
203-743-0
NACRES:
NA.21
MDL number:
Beilstein/REAXYS Number:
605763
Organoleptic:
odorless
Grade:
FG, Halal, Kosher
Biological source:
synthetic
Food allergen:
no known allergens
biological source
synthetic
grade
FG, Halal, Kosher
reg. compliance
FDA 21 CFR 117, FDA 21 CFR 172.350, FDA 21 CFR 175.105, EU Regulation 1334/2008 & 178/2002
vapor pressure
1.7 mmHg ( 165 °C)
assay
≥98%
form
powder or crystals
autoignition temp.
1364 °F
expl. lim.
40 %
mp
298-300 °C (subl.) (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
odorless
SMILES string
OC(=O)\C=C\C(O)=O
InChI
1S/C4H4O4/c5-3(6)1-2-4(7)8/h1-2H,(H,5,6)(H,7,8)/b2-1+
InChI key
VZCYOOQTPOCHFL-OWOJBTEDSA-N
Application
Fumaric acid is commonly used as a flavoring agent in food industries because of its sour, or acidic flavor. It has low water solubility. In order to increase its application in various foods, fumaric acid is used along with dioctyl sodium sulfosuccinate, a wetting agent.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
523.4 °F
flash_point_c
273 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
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The implication of organic acids in Pb translocation was studied in two species varying in shoot lead accumulation, Sesuvium portulacastrum and Brassica juncea. Citric, fumaric, malic and α-cetoglutaric acids were separated and determined by HPLC technique in shoots, roots and
Global Trade Item Number
| SKU | GTIN |
|---|---|
| W248800-1KG-K | 04061834323037 |
| W248800-25KG-K | 04061835518555 |
| W248800-SAMPLE-K | 04061834355281 |
