Isoamyl gallate

HCID 75596CAS 2486-02-4
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Basic information

Standard SMILES
CC(C)CCOC(=O)c1cc(O)c(O)c(O)c1
InChIKey
YBMTWYWCLVMFFD-UHFFFAOYSA-N
Molecular formula
C12H16O5
Average molar mass
240.25 g/mol
Monoisotopic mass
240.09977361

Overview

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Names & identifiers

Preferred name
Isoamyl gallate
IUPAC
3-methylbutyl 3,4,5-trihydroxybenzoate
English name
EC 1.4.1.3
Molecular formula
NULL
Molecular weight
0

Names & synonyms

ISOAMYL GALLATE2486-02-4Isopentyl gallateBenzoic acid, 3,4,5-trihydroxy-, 3-methylbutyl esterR0N2645G7IDTXSID50179558ISOPENTYL ALCOHOL, GALLATEGALLIC ACID, ISOAMYL ESTEREINECS 219-626-2GALLIC ACID, ISOPENTYL ESTERRefChem:791546DTXCID10102049
Show more names
GLUTAMATE DEHYDROGENASEGLDHGIDHL-GLDHGLDH-HAC:C&B33EC 1.4.1.4EC 1.4.1.3EC 1.4.1.2rGLDH(NADP)
219-626-2Gallic Acid Isoamyl Ester3-methylbutyl 3,4,5-trihydroxybenzoateIsopentyl 3,4,5-trihydroxybenzoateMFCD00016431iso-Amyl gallateGallicAcidIsoamylEster9029-11-2

Database identifiers

CAS
2486-02-4、9029-11-2
PubChem CID
75596
DTXSID
DTXSID50179558
UNII
R0N2645G7I
EC Number
219-626-2
Nikkaji
J191.973C

Properties

Computed structural properties

XLogP
2.8
Topological polar surface area
87 Ų
Hydrogen bond donors
3
Hydrogen bond acceptors
5
Rotatable bonds
5
Heavy atoms
17

Experimental & physicochemical properties

LogP2.8
Endocrine DisruptorsPotential endocrine disrupting compound

Physicochemical properties

storage temp.
2 · 2-8°C
form
solution (viscous)
color
amber
biological source
bacterial (Proteus spp.)
Specific Activity
50 · 50-200units/mg protein
UNSPSC Code
12352204 · 12352204

Safety & regulation

GHS classification

GHS ClassificationNot Classified

Hazard information

Hazard Classes and CategoriesNot Classified

Safety data

F
3-10
PPE
Eyeshields, Gloves, type N95 (US)
wgk
3
hs_code
35079090
safety_code
24/25
Storage Class
11 - Combustible Solids

Chemistry & industry

Uses & manufacturing

Use ClassificationFood Additives -> ANTIOXIDANT -> JECFA Functional Classes
Applications · 1 item

UsesThis enzyme is useful for enzymatic determination of NH3, α-ketoglutaric acid and L-glutamic acid, and for assay of leucine aminopeptidase and urease. This enzyme is also used for enzymatic determination of urea when coupled with urease (URH-201) in clinical analysis. In vitro, various activity assays of this enzyme examine the conversion of α-ketoglutarate to L-glutamate, in the presence of excess ammonium ions (NH4+) and NADPH.

Suppliers34 total

梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海麦克林生化科技股份有限公司021-50706066 15221275939 · [email protected]
Baoji Guokang Healthchem co.,ltd+8615604608665 15604608665 · [email protected]
Aladdin Scientific[email protected]
安耐吉化学&3A（安徽泽升科技股份有限公司）400-0056266 · [email protected]

Related reactions

1 records
New reaction record

Linked notes

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