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Key Documents

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Safety Information

68986

Supelco

Dimethyl disulfide

analytical standard

Synonym(s):

DMDS, Methyl disulfide

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100 MG
¥1,357.05

¥1,357.05

Available to ship on2025年4月23日Details

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100 MG
¥1,357.05

About This Item

Linear Formula:
CH3SSCH3
CAS Number:
624-92-0
Molecular Weight:
94.20
Beilstein:
1730824
EC Number:
210-871-0
MDL number:
MFCD00008561
UNSPSC Code:
85151701
PubChem Substance ID:
329761295
NACRES:
NA.24

¥1,357.05

Available to ship on2025年4月23日Details

Request a Bulk Order

grade

analytical standard

Quality Level

100

vapor density

3.24 (vs air)

vapor pressure

22 mmHg ( 20 °C)

Assay

≥98.5% (GC)

autoignition temp.

>572 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

16 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

impurities

≤0.5% water

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氟磷酸二异丙酯

D0879

氟磷酸二异丙酯

苯甲磺酰氟 ≥98.5% (GC)

P7626

苯甲磺酰氟

N-对-甲苯磺酰基-L-苯基乙基氯甲基酮 ≥97% (TLC), powder

T4376

N-对-甲苯磺酰基-L-苯基乙基氯甲基酮

乙酸异丙酯 ≥99.6%

537462

乙酸异丙酯

Gene Information

human ... ACHE(43), PTGS1(5742), PTGS2(5743)

Gene Information

-

Gene Information

human ... NFKB1(4790), NKAP(79576), NKRF(55922), NOS2(4843), PTGS2(5743)

Gene Information

-

Quality Level

100

Quality Level

300

Quality Level

200

Quality Level

200

form

liquid

form

powder

form

powder

form

liquid

solubility

anhydrous isopropanol: 0.1-0.5 M (stable for months if stored at -70 °C), H2O: 1.5% at 25 °C (very unstable (at pH 7.5, half-life = 1 hr); decomposed by alkali.)

solubility

dry solvents (ethanol, methanol, and 2-propanol): 200 mM (Stock solution are stable for months at 4°C.), H2O: unstable

solubility

DMSO: >10 mg/mL (stable for several months at 4°C.), ethanol: 20 mg/mL

solubility

water: soluble 31.9 g/L at 20 °C

storage temp.

2-8°C

storage temp.

-

storage temp.

−20°C

storage temp.

-

General description

Dimethyl disulfide is an organic disulfide, and a commonly used potent odorant which contributes to the aroma in heated food products.[1]

Application

Dimethyl disulfide may be used as an analytical reference standard for the quantification of the analyte in commercial garlic products using high-performance liquid chromatography.[2]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Sens. 1 - STOT SE 1 Inhalation - STOT SE 3

Target Organs

Central nervous system, Upper respiratory tract

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

59.0 °F - closed cup

Flash Point(C)

15 °C - closed cup

Regulatory Information

危险化学品
  • Specification Sheet

    • Choose from one of the most recent versions:

    Certificates of Analysis (COA)

    Lot/Batch Number
    BCCM9588
    BCCM4016
    BCCL8262
    BCCL9016
    BCCH7720

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    Identification and HPLC quantitation of the sulfides and dialk (en) yl thiosulfinates in commercial garlic products
    Lawson.DL, et al.
    Planta Medica, 57(04), 363-370 (1991)
    An Overview of the Contribution of Sulfur-Containing Compounds to the Aroma in Heated Foods
    Mottram.SD and Mottram.RH
    ACS Symp. Ser., 826 (2002)
    M N Kardar et al.
    Phytochemistry, 106, 156-163 (2014-08-12)
    Chemical investigation of a sample of propolis originating from North-Western Cameroon led to the isolation of thirteen alk(en)ylphenols (1-13) (inseparable mixture) along with α-amyrin (14), β-amyrin (15), lupeol (16), cycloartenol (17), mangiferonic acid (18), ambonic acid (19), mangiferolic acid (20)
    Esther Vega et al.
    Chemosphere, 109, 113-119 (2014-05-31)
    The effectiveness of different advanced oxidation processes on the treatment of a multicomponent aqueous solution containing ethyl mercaptan, dimethyl sulphide and dimethyl disulphide (0.5 mg L(-1) of each sulphur compound) was investigated with the objective to assess which one is
    Gizem Keceli et al.
    Biochemistry, 53(22), 3689-3698 (2014-05-30)
    Nitroxyl (HNO), a potential heart failure therapeutic, is known to target cysteine residues to form sulfinamides and/or disulfides. Because HNO-derived modifications may depend on their local environment, we have investigated the reactivity of HNO with cysteine derivatives and C-terminal cysteine-containing
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