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线性分子式:
2-(HO)C6H4CO2C6H5
化学文摘社编号:
分子量:
214.22
Flavis number:
9.689
PubChem Substance ID:
UNSPSC Code:
12164502
FEMA Number:
3960
NACRES:
NA.21
EC Number:
204-259-2
MDL number:
Beilstein/REAXYS Number:
393969
Organoleptic:
fruity; sweet
Grade:
FG
Biological source:
synthetic
Agency:
meets purity specifications of JECFA
Food allergen:
no known allergens
产品名称
水杨酸苯酯, ≥99%, FG
InChI key
ZQBAKBUEJOMQEX-UHFFFAOYSA-N
InChI
1S/C13H10O3/c14-12-9-5-4-8-11(12)13(15)16-10-6-2-1-3-7-10/h1-9,14H
SMILES string
Oc1ccccc1C(=O)Oc2ccccc2
biological source
synthetic
grade
FG
agency
meets purity specifications of JECFA
reg. compliance
EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 110
assay
≥99%
bp
172-173 °C/12 mmHg (lit.)
mp
41-43 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
fruity; sweet
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signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
J Baran et al.
Physical review. E, Statistical, nonlinear, and soft matter physics, 81(3 Pt 1), 031503-031503 (2010-04-07)
We report the investigation of glass-forming salol upon different courses of the temperature changes from liquid to glass state and back using FT-IR spectroscopy measurements in the wide spectral and temperature ranges. The formation of the ordered clusters in supercooled
Cross-sensitivity between resorcinol, resorcinol monobenzoate and phenyl salicylate.
M Nakagawa et al.
Contact dermatitis, 27(3), 199-200 (1992-09-01)
C D Calnan et al.
Contact dermatitis, 7(4), 208-211 (1981-07-01)
Six cases of contact dermatitis from a lip salve are described. Five were allergic to phenyl salicylate and one to geraniol in the fragrance. The dermatitis spread in a ring around the mouth. Phenyl salicylate has been removed from the
P T Deota et al.
Natural product research, 17(1), 21-26 (2003-04-04)
The effect of photostabilization of azadirachtin-A (Aza-A) was examined in solutions when exposed to UV radiation, in the presence of four structurally different UV absorbers namely, p-aminobenzoic acid, 2,4-dihydroxybenzophenone, 4,4'-dihydroxybenzophenone and phenyl salicylate. The percentages of Aza-A recovered from the
Allergic contact dermatitis to various salols (phenyl salicylates). A structure-activity relationship study in man and in animal (guinea pig).
B Marchand et al.
Archives of dermatological research, 272(1-2), 61-66 (1982-01-01)
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