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线性分子式:
CH3CH2CH2C6H4OH
化学文摘社编号:
分子量:
136.19
FEMA Number:
3522
Council of Europe no.:
11908
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
4.046
EC Number:
211-415-3
NACRES:
NA.21
MDL number:
SMILES string
CCCc1ccccc1O
InChI
1S/C9H12O/c1-2-5-8-6-3-4-7-9(8)10/h3-4,6-7,10H,2,5H2,1H3
InChI key
LCHYEKKJCUJAKN-UHFFFAOYSA-N
biological source
synthetic
grade
FG, Fragrance grade
agency
follows IFRA guidelines
reg. compliance
EU Regulation 1223/2009, EU Regulation 1334/2008 & 872/2012, FDA 21 CFR 110
assay
≥97%
refractive index
n20/D 1.527 (lit.)
bp
224-226 °C (lit.)
density
0.989 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
fragrance allergen
no known allergens
organoleptic
medicinal; phenolic
Quality Level
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
199.4 °F - closed cup
flash_point_c
93 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
H P Kohler et al.
Applied and environmental microbiology, 59(3), 860-866 (1993-03-01)
A mutant of Pseudomonas sp. strain HBP1, originally isolated on 2-hydroxybiphenyl, was selected for the ability to grow on 2-propylphenol as the sole carbon and energy source. In the mutant strain, which was designated as Pseudomonas sp. strain HBP1 Prp
M C Jaspers et al.
Journal of bacteriology, 182(2), 405-417 (2000-01-12)
The regulation of 2-hydroxybiphenyl and 2,2'-dihydroxybiphenyl degradation in Pseudomonas azelaica is mediated by the regulatory gene, hbpR. The hbpR gene encodes a 63-kDa protein belonging to the NtrC family of prokaryotic transcriptional activators and having the highest homology to members
Cynthia D Selassie et al.
Journal of medicinal chemistry, 48(23), 7234-7242 (2005-11-11)
In this comprehensive study on the caspase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L1210), we determined the concentrations needed to induce caspase activity by 50% (I50) and utilized these data to develop the following
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