推荐产品
生物源
synthetic
品質等級
等級
Kosher
agency
meets purity specifications of JECFA
蒸汽密度
3.1 (vs air)
蒸汽壓力
83 mmHg ( 37.7 °C)
化驗
≥98%
折射率
n20/D 1.443 (lit.)
bp
98 °C (lit.)
mp
−116 °C (lit.)
密度
0.842 g/mL at 25 °C (lit.)
應用
flavors and fragrances
文件
see Safety & Documentation for available documents
食物過敏原
no known allergens
感官的
sulfurous
SMILES 字串
CCCCS
InChI
1S/C4H10S/c1-2-3-4-5/h5H,2-4H2,1H3
InChI 密鑰
WQAQPCDUOCURKW-UHFFFAOYSA-N
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一般說明
1-Butanethiol is a volatile sulfur-containing odorous compound that is reported to occur in skunk oil.
免責聲明
For R&D or non-EU Food use. Not for retail sale.
訊號詞
Danger
危險分類
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
53.6 °F - closed cup
閃點（°C）
12 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
The history of skunk defensive secretion research.
Wood WF
The Chemical Educator, 4(2), 44-50 (1999)
Nicole W G Smits et al.
Inorganic chemistry, 58(19), 13007-13019 (2019-09-25)
The structure of the copper complex of the 6-((1-butanethiol)oxy)-tris(2-pyridylmethyl)amine ligand (Cu-tmpa-O(CH2)4SH) anchored to a gold surface has been investigated. To enable covalent attachment of the complex to the gold surface, a heteromolecular self-assembled monolayer (SAM) of butanethiol and a thiol-substituted
Rosanna Toniolo et al.
Analytical and bioanalytical chemistry, 405(11), 3571-3577 (2012-12-13)
A prototype of a fast-response task-specific amperometric gas sensor based on paper-supported room-temperature ionic liquids (RTILs) is proposed here for improved analysis of volatile acid species. It consists of a small filter paper foil soaked with a RTIL mixture containing
E Mather-Mihaich et al.
Comparative biochemistry and physiology. C, Comparative pharmacology and toxicology, 85(2), 427-432 (1986-01-01)
Indicators of free-radical or oxidant-mediated responses were quantified in channel catfish, Ictalurus punctatus, exposed to the organophosphorus herbicide DEF and its metabolite, n-butyl mercaptan (nBM). The activities of the antioxidant enzymes superoxide dismutase (SOD), glutathione peroxidase (GPX) and catalase did
Late acute, delayed neurotoxic and cholinergic effects of S,S,S-tributyl phosphorotrithioite (Merphos) in hens.
M B Abou-Donia et al.
Toxicology and applied pharmacology, 53(3), 439-457 (1980-05-01)
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